Browse Device Recalls
7 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 7 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 7 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Mar 9, 2026 | LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number... | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subs... | Class II | LSL Healthcare Inc. |
| Mar 9, 2026 | LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131 | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subs... | Class II | LSL Healthcare Inc. |
| Mar 9, 2026 | LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subs... | Class II | LSL Healthcare Inc. |
| Mar 9, 2026 | LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Numb... | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subs... | Class II | LSL Healthcare Inc. |
| Mar 9, 2026 | LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555 | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subs... | Class II | LSL Healthcare Inc. |
| Mar 9, 2026 | LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554 | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subs... | Class II | LSL Healthcare Inc. |
| Dec 22, 2025 | LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medi... | BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packagi... | Class II | LSL Healthcare 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.