Arthrex, Inc. recalls K-Wire, 1.35 mm x 170 mm
See all recalls from Arthrex, Inc. →Recalled Product
K-Wire, 1.35 mm x 170 mm
Hazard / Issue
Products do not meet length and diameter specifications.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084
✅ 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 K-Wire, 1.35 mm x →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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