Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog #25-3011, Lot #1049402
- 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:
- ArthroCare Medical Corporation
- Reason for Recall:
- A sharp edge on the cannulated tip of the device may damage or cut a suture.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Product Codes/Lot Numbers:
Catalog #25-3011, Lot #1049402
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0652-2014
Related Recalls
Potential component failure causing device inoperability
Potential component failure resulting in inoperability
The recalling firm was notified by the contract manufacturer that they had reversed the L2, L3, L4, or L5 components on the P/N09010 RoHS boards of the Coblator II Controller (Model RF8000E).