Browse Device Recalls
5 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 5 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 5 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| May 28, 2021 | Stimulen Collagen Moisturizing Lotion, ST9555B | Dose audit failure after sterilization process | Class II | Southwest Technologies Inc |
| Nov 18, 2019 | Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Ster... | Elasto-Gel Wound Dressing may be contaminated with mold. | Class II | Southwest Technologies Inc |
| Dec 28, 2017 | HYPOTHERMIA MITTS Supportive in Cancer, packaged under the following brands: ... | Hypothermia mitts, hypothermia slippers, and hypothermia caps on the market are misbranded for us... | Class II | Southwest Technologies Inc |
| Dec 28, 2017 | HYPOTHERMIA SLIPPERS Supportive in Cancer, packaged under the following brand... | Hypothermia mitts, hypothermia slippers, and hypothermia caps on the market are misbranded for us... | Class II | Southwest Technologies Inc |
| Dec 28, 2017 | HYPOTHERMIA CAP Supportive in Cancer, packaged under the following brands: (... | Hypothermia mitts, hypothermia slippers, and hypothermia caps on the market are misbranded for us... | Class II | Southwest Technologies 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.