Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and… — Class II medical device recall Z-1356-2020
Terminated recall by Zimmer Surgical Inc, reported 2020-03-04, distributed nationwide. When inflating/deflating a single bladder, both bladders could potentially inflate/deflate due to a leak betwe
| Recall number | Z-1356-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Surgical Inc, Dover, OH, United States |
| Recall initiated | 2020-01-03 |
| Classified | 2020-02-25 |
| Reported by FDA | 2020-03-04 |
| Terminated | 2020-10-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | NL |
| Quantity | 58 |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00889024377547 |
| Lot numbers | 27968701 |
| Model numbers | 60708015200 |
Product
Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field.
Reason for recall
When inflating/deflating a single bladder, both bladders could potentially inflate/deflate due to a leak between the bladders.
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-1356-2020. 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.