Browse Device Recalls
12 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 12 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 12 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Apr 15, 2016 | Volt Resistance Heated Lower Back Garment Deep penetrating heat garment and ... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment and w... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep penetra... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment a... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment and w... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat garme... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment an... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat garmen... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat garm... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations Inc. |
| Apr 15, 2016 | Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment and w... | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims ... | Class II | 2k Innovations 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.