Medical devices
Shortlist up to four to read them side by side.
2,589 medical device recalls FDA’s Enforcement Report published in 2026, the newest year, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 6, 2026.
2,589of 2,589 medical device recallsshown with your filters
The list
- Medical device recall Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: DRAINAGE KIT/AK-01600, DRAINAGE KIT/AK-01601, DRAINAGE KIT/ASK-01601-MM, THORACENTESIS… Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: ACCESS TRAY/ASK-04001-JHH Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: ACCESS TRAY/GU-04020 Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PARACENTESIS KIT/ASK-00376-JHH Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3L 12 FR X 16… Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: ACCESS TRAY/ASK-04001-MC3 Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedJun 24, 2026ClassClass IStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Philips MultiDiagnost Eleva with the following Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended… Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Philips Allura Xper with the following Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended… Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline EBSI Kit EBSI1534 Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C DYNJ900004J DYNJ901779J DYNJ902900F EAR… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ENDO BREAST AUGMENTATION PACK… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662 Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359 Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B MRI DBS PACK DYNJ9814630O NEURO… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kit Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: WT LAVH PACK DYNJ46609F Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: DAVINCI MAIN DYNJ908031D Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX… Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Class IIFDA’s classJun 24, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 24, 2026ClassClass IIStatusOngoingWhereNationwide
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Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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