Brasseler USA, Medical L.L.C.: Medical Device Recall in 2022 - (Recall #: Z-0707-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S

Product Classification:

Class II

Date Initiated: January 28, 2022

Date Posted: March 9, 2022

Recall Number: Z-0707-2022

Event ID: 89555

Reason for Recall:

One lot of product was distributed in unsealed packaging

Status: Terminated

Product Quantity: 231 units

Code Information:

UDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX

Distribution Pattern:

US Nationwide distribution in the states of OH, MI, AZ, FL, CA, TN, TX, SC, PA IL, ID.

Voluntary or Mandated:

Voluntary: Firm initiated