Browse Device Recalls
4 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 4 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 4 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Mar 27, 2023 | TDHisto/Cyto - A software product used for managing medical information in th... | In a specific use case, when printing labels for slides, some labels may display wrong information | Class II | Technidata S.A. |
| Feb 17, 2014 | TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkst... | If a conflict occurs between a Demography Query and a Result Transmission by the instrument, the ... | Class III | Technidata S.A. |
| Jun 20, 2013 | TDHistology/Cytology Classification name: Calculator/data processing modul... | A recall was initiated by Technidata because use of symbols (less than or equal to or greater tha... | Class III | Technidata S.A. |
| Jul 29, 2010 | TD-Synergy. Laboratory Information System. | Technidata has discovered that using the F8 key in the ERM session to add a combined test can res... | Class II | Technidata S.A. |
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.