REF: 60-7070-005 — Class II medical device recall Z-2405-2024
Ongoing recall by Stryker Sustainability Solutions, reported 2024-07-24, distributed nationwide. Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff sing
| Recall number | Z-2405-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2024-05-31 |
| Classified | 2024-07-17 |
| Reported by FDA | 2024-07-24 |
| Distributed | Nationwide (US) |
| Quantity | 90 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00885825015411 |
| Lot numbers | 0000564862 |
| Model numbers | 60-7070-005 |
Product
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Reason for recall
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
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-2405-2024. 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.