Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Class I - DangerousWhat Should You Do?
- Check if you have this product: lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597
- 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:
- Aesculap, Inc.
- Reason for Recall:
- The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Product Codes/Lot Numbers:
lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597
Distribution:
Distributed in: FL, MD
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0492-2014
Related Recalls
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.