Arthrex, Inc. recalls Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used i
See all recalls from Arthrex, Inc. →Recalled Product
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Hazard / Issue
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Product Code AR-8770-02, Lot Number 032052
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Drill Bit, Cannulated, 5.0 →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime