FDAFDA · Food and drugs·Recall number Z-1113-2017
Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Published February 8, 2017 · Recall initiated: December 22, 2016
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
The product is being recalled due to incidence and reports of the product breaking during surgery.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Flower Orthopedics Corporation
- Distributor
- Distributed throughout the United States
- Lot
- Device Listing: D267957
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.