Brasseler USA — Class II medical device recall Z-0707-2022
Terminated recall by Brasseler USA, Medical L.L.C., reported 2022-03-09, distributed nationwide. One lot of product was distributed in unsealed packaging
| Recall number | Z-0707-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Brasseler USA, Medical L.L.C., Savannah, GA, United States |
| Recall initiated | 2022-01-28 |
| Classified | 2022-03-01 |
| Reported by FDA | 2022-03-09 |
| Terminated | 2023-02-03 |
| Distributed | Nationwide (US) |
| Quantity | 231 units |
| UPC / GTIN / UDI-DI | 00887919491033 |
| Lot numbers | NV1MX |
| Model numbers | KM172-26-35S |
Product
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Reason for recall
One lot of product was distributed in unsealed packaging
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-0707-2022. 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.