FDA Device recall Z-0707-2022
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
- FDA Device
- Class II
- terminated
- Published 2022-03-09
On 2022-03-09 the FDA classified a Class II recall of Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S by Brasseler Usa Medical, citing one lot of product was distributed in unsealed packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0707-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-01-28 |
| Published | 2022-03-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Brasseler Usa Medical |
| Distribution | US |
Product
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Reason
One lot of product was distributed in unsealed packaging
Identifiers
| code_info | UDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0707-2022%22
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