CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot # 0061536043 Exp: 8/31/2018 Lot # 0061620273 Exp:11/30/2019 UDI: 04046964941399
- 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:
- B. Braun Medical, Inc.
- Reason for Recall:
- The filter capacity is not achieved due to damage of the filter membrane.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
Product Codes/Lot Numbers:
Lot # 0061536043 Exp: 8/31/2018 Lot # 0061620273 Exp:11/30/2019 UDI: 04046964941399
Distribution:
Distributed in: CA, FL, MO, TX, MN, AL, GA, NC, IL, PA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2470-2019
Related Recalls
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.