FDAFDA · Food and drugs·Recall number Z-0652-2014
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Published January 15, 2014 · Recall initiated: December 9, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
A sharp edge on the cannulated tip of the device may damage or cut a suture.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- ArthroCare Medical Corporation
- Distributor
- Worldwide distribution: US (nationwide) including states of: CA, FL, GA, IL, IN, KY, MN, MO, NY, OH, TX, and WI. Internationally to: Canada, France, Germany, Spain, and Switzerland.
- Lot
- Catalog #25-3011, Lot #1049402
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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