Medical devices, 2013
Shortlist up to four to read them side by side.
2,249 medical device recalls FDA’s Enforcement Report published in 2013, 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.
2,249of 2,249 medical device recallsshown with your filters
The list
- Medical device recall BD Vacutainer Buffered Sodium Citrate BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood Collection Tube due to extended Partial Thromboplastin Time (aPTT) test results… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Brand Name: RX Accunet Embolic Protection System Common Name: RX Accunet EPS The recall was initiated because Abbot Vascular has discovered that the identified lots of the RX Accunet Embolic Protection System may exhibit difficult… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ethicon Endo-Surgery Inc Potential for self activation while the device is in use, which may result in unintended thermal damage. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement Report46 statesnamed in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereAlaska, 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, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Rectal Retractors, stainless steel A medical device used in brachytherapy may become contaminated and can cause infections, toxicity or allergic reactions. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Rectal Retractors, titanium A medical device used in brachytherapy may become contaminated and can cause infections, toxicity or allergic reactions. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall COBAS TaqMan Mycobacteria tuberculosis (MTB) Test FOR IN VITRO DIAGNOSTIC USE. The COBAS TaqMan MTB Test Definition Files (TDF) v3.0, for both CE-IVD and JPN-IVD tests, being used with AMPLILINK software version 3.3 series and COBAS… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNot namedno state, in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator’s Manual Product… The firm is adding an addendum to the operator’s manual for Infinity Enteralite Ambulatory Feeding Pumps pertaining to the Infinite Dose mode and the inability… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer. A software security issue with Oracles TNS-Listener component has been identified. Class IIIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 46 states named PublishedJan 30, 2013ClassClass IIIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Connecticut, District of Columbia, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, 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 and Wyoming named
- Medical device recall Abbott Laboratories, ARCHITECT 25-OH Vitamin D Reagent Kit, 03L52-25 (ROW) and 03L52-27 (U.S.) The Architect 25-OH Vitamin D assay has the potential to generate falsely elevated or falsely depressed results when used with certain lots of Architect… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Becton, Dickinson and Company, BBL Crystal Enteric/Nonfermenter ID Kit In-vitro diagnostic reagents for microbiological testing may be reversed in well positions in the test kit and when utilized may lead to bacteria… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement Report14 statesnamed in where it went PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereArizona, California, Florida, Georgia, Indiana, Kentucky, Massachusetts, Michigan, North Carolina, New Jersey, New York, Tennessee, Texas and Washington
- Medical device recall GreenLight HPS (High Performance System) GreenLight XPS (Xcelerated Performance System) During electrical recertification testing it was found that the Voltage Scaling Board was non-conforming to the IEC 60601-1-2 standard. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Becton, Dickinson and Company, BD MAX (tm) Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement Report12 statesnamed in where it went PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereConnecticut, Florida, Illinois, Kansas, Maryland, Michigan, Missouri, New York, Pennsylvania, Rhode Island, Texas and Wisconsin
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank… Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Polyaxial screws 8x 80 and larger may disassociate when inserting in the ilium. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Hawaii, Illinois, Maryland, Michigan, Missouri, North Carolina, Tennessee and Texas named
- Medical device recall Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1” instead of 15 Ga x 3/5”. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and New York, Pennsylvania and Tennessee named
- Medical device recall Medisystems 17 Gauge x 1” inch AV Fistula Needle Single needle packs in each case ( 10 needles per case) are mislabeled on the pouch as 15 Gauge needles instead of 17 Gauge Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and New York, Pennsylvania and Tennessee named
- Medical device recall Abbott Point of Care i-Stat cTnI cartridge APOC has determined that 10 boxes of i-Stat cTnI cartridges from lot P12179 have an incorrect barcode applied to the cartridge portion pack. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of Ultra Sensitive, Flavors and… One lot of Lifestyles Pleasure Collection Lubricated Condoms is misbranded. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP, Disposable Hyfrecator(R) Tips, REF/Catalog No. 7-100-8CS,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT, Disposable Hyfrecator(R) Tips, REF/Catalog No. 7-101-8CS,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Goldvac(TM) UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended Insulation, REF/Catalog No.… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended Insulation, REF/Catalog No.… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Goldvac(TM) UltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 60-7524-001, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade, REF/Catalog No. 60-7526-001, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall ABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece), REF/Catalog No.… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall TUR/Endoscopic Cable, 10 feet ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall CONMED(R) ELECTROSURGICAL SAFETY HOLSTER, Disposable Safety Holster, REF/Catalog No. 137668, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall ELECTROSURGICAL ENT NEEDLE ELECTRODE, 6 inch with Extended Insulation, REF/Catalog No. 138025, Single Use,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Electrosurgical Tip Cleaner, REF/Catalog No. 138029, Single Use, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode, 1 inch Coated Blade, REF/Catalog No. 139100, Single Use, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 1 inch Coated Needle, REF/Catalog No. 139102, Single Use, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended Insulation, REF/Catalog No. 139104EXT,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended Insulation, REF/Catalog No. 139105EXT,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 6 inch Coated Blade, REF/Catalog No. 139107, Single Use, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 6 inch Coated Needle with Extended Insulation, REF/Catalog No. 139108,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended Insulation, REF/Catalog No. 139110EXT,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 139112, Single Use, Sterile ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended Insulation, REF/Catalog No. 139112EXT,… ConMed received complaints of some devices which had broken through the seal of the sterile pouch. Class IIFDA’s classJan 30, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 30, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Sarns flexible arterial cannula, 6.7 mm Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were identified to contain flash on the exterior of the cannula connector that exceeded… Class IIFDA’s classJan 23, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJan 23, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Missouri, North Carolina, North Dakota, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Sarns flexible arterial cannula, 7.3 mm Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were identified to contain flash on the exterior of the cannula connector that exceeded… Class IIFDA’s classJan 23, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJan 23, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Missouri, North Carolina, North Dakota, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Sarns flexible arterial cannula, 8.0 mm Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were identified to contain flash on the exterior of the cannula connector that exceeded… Class IIFDA’s classJan 23, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJan 23, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Missouri, North Carolina, North Dakota, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
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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