Zimmer Tourniquet Cuff 30" — Class II medical device recall Z-1802-2020
Terminated recall by Stryker Sustainability Solutions, reported 2020-05-06, distributed nationwide. Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadeq
| Recall number | Z-1802-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2019-10-09 |
| Classified | 2020-04-27 |
| Reported by FDA | 2020-05-06 |
| Terminated | 2021-01-14 |
| Distributed | Nationwide (US) |
| Quantity | 90 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00885825013868 |
| Lot numbers | 10237165 |
| Model numbers | 60-7070-105 |
Product
Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Product Usage: Reprocessed tourniquet cuffs are indicated for use in patients who require surgery of the extremities with an expected duration of less than 90 minutes when temporary exsanguination of a limb is desired.
Reason for recall
Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.
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-1802-2020. 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.