Recalls / —
—#177473
Product
PRO-STIM 10cc INJECTABLE, Part Number 86SR0410
- FDA product code
- MBP — Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
- Device class
- Class 2
- Medical specialty
- Orthopedic
- 510(k) numbers
- K083270
- Affected lot / code info
- Lot Number 1564697
Why it was recalled
The firm discovered a lack of adequate documentation confirming sterility on certain products.
Root cause (FDA determination)
Process control
Action the firm took
The firm initiated the recall on 11/08/2016 by letter and email to the user level. The firm requested the return of the units.
Recalling firm
- Firm
- Wright Medical Technology, Inc.
- Address
- 11576 Memphis Arlington Rd, Arlington, Tennessee 38002-9497
Distribution
- Distribution pattern
- US and Norway, Italy, Germany, France, South Africa, UK, Taiwan, Austria, Japan, Turkey, Denmark, Canada, Switzerland, Belgium, The Netherlands, Spain
Timeline
- Recall initiated
- 2016-11-08
- Terminated
- 2020-11-03
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #177473. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.