Brand Name: Zimmer Tourniquet Systems Product Name: A — Class II medical device recall Z-1201-2026
Ongoing recall by Zimmer Surgical Inc, reported 2026-02-04. Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-Englis
| Recall number | Z-1201-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Surgical Inc, Dover, OH, United States |
| Recall initiated | 2025-12-24 |
| Classified | 2026-01-28 |
| Reported by FDA | 2026-02-04 |
| Countries outside the US | CA |
| Quantity | 206 |
| UPC / GTIN / UDI-DI | 00889024626454, 50066722609001, 50066722611004, 50066742892001, 50066742893008, 50066742893015, 50066751087009, 50066751087016, 50066848799006, 50066848799013, 50066848799020, 50066870330017, 50067046298018, 50067117765005, 50067117766002, 50067117768006, 50067117768013, 50067482667003, 50067482667010, 50067553349012 |
| Lot numbers | 66722609, 66722610, 66722611, 66742892, 66742893, 66751087, 66848797, 66848799, 66870330, 66959543, 66969025, 66969027, 66995371, 67046297, 67046298, 67071240, 67117765, 67117766, 67117768, 67482667, 67533336, 67542546, 67553349 |
| Serial numbers | 50066722609001, 50066722609002, 50066722609003, 50066722609004, 50066722609005, 50066722610001, 50066722610002, 50066722610003, 50066722610004, 50066722610005, 50066722611001, 50066722611002, 50066722611003, 50066722611004, 50066722611005, 50066722611006, 50066722611007, 50066722611008, 50066722611009, 50066722611010, 50066742892001, 50066742892002, 50066742892003, 50066742892004, 50066742892005 and 181 more |
| Model numbers | 60500010100 |
Product
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are within scope of the recall for A.T.S.¿ 5000TS Product Description: A.T.S 5000TS Tourniquet Systems Component: N/A
Reason for recall
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1201-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.