Arthrex, Inc. recalls Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Pr
See all recalls from Arthrex, Inc. →Recalled Product
Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and fractures of the proximal tibia and distal femur.
Hazard / Issue
It was discovered that five AR-13200ST-15.0 parts were processed as AR-13200T-15.0 parts.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Part number: AR-13200T-15.0; Lot code:12135408
✅ 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 Tibial Opening Wedge Osteotomy →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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