Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Class I - Dangerous 🏥 Medical Devices
Recalled: January 28, 2022 Brasseler USA, Medical L.L.C. Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: UDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Brasseler USA, Medical L.L.C.
- Reason for Recall:
- One lot of product was distributed in unsealed packaging
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Product Codes/Lot Numbers:
UDI (01)00887919491033(17)260719(10)NV1MX Lot Code NV1MX
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0707-2022