Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S — FDA record Z-0707-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 28, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Reason
One lot of product was distributed in unsealed packaging
Classification
Class II
Recalling firm
Brasseler USA, Medical L.L.C.
Quantity
231 units
Agency-reported status
Terminated
Source record identifier
Z-0707-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Mar 9, 2022
Recall initiation date
Jan 28, 2022
Center classification date
Mar 1, 2022
Termination date
Feb 3, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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