# FDA recall Z-0707-2022

> **Brasseler USA, Medical L.L.C.** · Class II · device recall initiated 2022-01-28.

## Product

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

## Reason for recall

One lot of product was distributed in unsealed packaging

## Distribution

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

## Key facts

- **Recall number:** Z-0707-2022
- **Recalling firm:** Brasseler USA, Medical L.L.C.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-01-28
- **Report date:** 2022-03-09
- **Termination date:** 2023-02-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Savannah, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0707-2022

## Citation

> AI Analytics. FDA recall Z-0707-2022. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-0707-2022. Source: US FDA. Licensed CC0.

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