Brasseler USA, Medical L.L.C. Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Brand
Brasseler USA, Medical L.L.C.
Lot Codes / Batch Numbers
UDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX
Products Sold
UDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX
Brasseler USA, Medical L.L.C. is recalling Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S due to One lot of product was distributed in unsealed packaging. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
One lot of product was distributed in unsealed packaging
Recommended Action
Per FDA guidance
The firm initiated the recall by telephone on 01/28/2022 and followed with a letter delivered by email. The letter explained the issue and requested the consignee set the affected product aside to be returned to the recalling firm.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026