Browse Device Recalls
8 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 8 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Medical Device Recalls
Browse 8 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Mar 26, 2020 | Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing cont... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Mar 26, 2020 | Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing hydroge... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Mar 26, 2020 | Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing cont... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Mar 26, 2020 | Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing cont... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Feb 27, 2020 | Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care ... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Feb 27, 2020 | Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care o... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Feb 27, 2020 | Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
| Feb 27, 2020 | Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care ... | During an FDA audit, it was discovered that the product was not properly registered with FDA. | Class II | Gentell, Inc |
Frequently Asked Questions
When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.
All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.
Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.