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 5, 2026.
2,589of 2,589 medical device recallsshown with your filters
The list
- Medical device recall JenaValve Trilogy Delivery Catheter, Size 27MM Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 18 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Georgia, Illinois, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New York, Ohio, Pennsylvania, South Carolina, Texas, Utah, Virginia and Washington named
- Medical device recall Grafton” DBM and Grafton Plus” DBM contain demineralized human bone tissue combined with an inert additive to… Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Colorado, Delaware, Florida, Georgia, Illinois, Kansas, Maryland, Michigan, Oklahoma, Texas and Virginia named
- Medical device recall Grafton” DBM and Grafton Plus” DBM contain demineralized human bone tissue combined with an inert additive to… Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Colorado, Delaware, Florida, Georgia, Illinois, Kansas, Maryland, Michigan, Oklahoma, Texas and Virginia named
- Medical device recall BD Phoenix Panel NMIC-312 Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BD Phoenix Panel NMIC-306 Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Brand Name: IOMAX Product Name: IOMAX Cortical Module Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Tennessee named
- Medical device recall NeuroStar Advanced Therapy System Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall NaviFlex LW Pusher Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 17 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, California, Florida, Georgia, Illinois, Indiana, Kentucky, Maryland, North Carolina, New Hampshire, New Mexico, New York, Rhode Island, Texas, Washington, Wisconsin and West Virginia named
- Medical device recall Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 10 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, Missouri, North Dakota, Ohio and Utah named
- Medical device recall Power F2 Powered Fastening System, Power F2 Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 30 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Florida, Idaho, Illinois, Kentucky, Louisiana, Maine, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall iFuse TORQ Implant System The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Florida, Georgia, Hawaii, North Carolina, Ohio, Pennsylvania, South Dakota, Texas and Virginia named
- Medical device recall FORWARD Gunshot Wound Kit Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device’s sterile pad, potentially causing the… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Georgia and Virginia named
- Medical device recall Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 48 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Guam, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 48 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Guam, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Generic Name: BioFire¿ Joint Infection (JI) Panel Generic Name: BioFire¿ Joint Infection (JI) Panel Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 48 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Guam, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Likorall Overhead Lifts Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 49 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, 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, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18” TF-5 Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 26 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arizona, California, Colorado, Florida, Idaho, Illinois, Indiana, Louisiana, Massachusetts, Maine, Minnesota, Missouri, North Carolina, Nebraska, New Hampshire, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Wisconsin and Wyoming named
- Medical device recall RAPICIDE PA Part A High-Level Disinfectant If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall RAPICIDE PA Part A High-Level Disinfectant If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall RAPICIDE PA Part A High-Level Disinfectant If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Florida, Georgia, Hawaii, North Carolina, Ohio, Pennsylvania, South Dakota, Texas and Virginia named
- Medical device recall Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis The potential for the devices to be mislabeled with the incorrect length. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Georgia and Rhode Island named
- Medical device recall MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1 Vial-to-vial variability in MAS¿ Omni”IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Louisiana, Michigan, Missouri, New York, Ohio, Oklahoma, Oregon, South Carolina, Texas and Utah named
- Medical device recall DxU 840m Iris The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however,… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 53 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Guam, 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 IQ200 SPRINT The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however,… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 53 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Guam, 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 LeadCare II Blood Lead Test Kit In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct… Class IIIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedOct 21, 2026ClassClass IIIStatusOngoingWhereNationwide, and California, Illinois, Indiana, Kentucky, Massachusetts, Missouri, Nebraska, Pennsylvania and Texas named
- Medical device recall Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and… The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement Report5 statesnamed in where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereFlorida, Illinois, New Mexico, Texas and Washington
- Medical device recall TS Universal Baseplate Finishing Tray, Triathlon Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall TS Femoral Prep Tray, Triathlon Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Triathlon Hinge Femoral Prep Tray Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall TS Misc. Instruments Tray, Triathlon. Catalog Number: 6543-6-519. Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall 1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) OPEN HEART CDS, Medline product number/SKU CDS840094R Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF, Medline product number/SKU… Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU… Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF, Medline Product number/SKU DYNJ0538615K Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product Number/SKU DYNJ80055A Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medline surgical convenience kits labeled as: 1) SPINAL CDS, Medline Product Number/SKU CDS940087AM Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to… Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660… Kits contain CONMED AirSeal Access Ports. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio and Wisconsin named
- Medical device recall Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258 KIT… Kits contain CONMED AirSeal Access Ports. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio and Wisconsin named
- Medical device recall Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071… Kits contain CONMED AirSeal Access Ports. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio and Wisconsin named
- Medical device recall Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY DYNJ906731K DYNJ906731L DYNJ906731N… Kits contain CONMED AirSeal Access Ports. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio and Wisconsin named
- Medical device recall Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY… Kits contain CONMED AirSeal Access Ports. Class IIFDA’s classOct 21, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedOct 21, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio 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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