Recall Z-1035-2022— Arthrex, Inc.
Class II · Ongoing
Class II FDA medical device recall by Arthrex, Inc., initiated 2022-03-25. FDA's recall record names no specific 510(k) clearance for this event. Product: K-Wire, 1.35 mm x 170 mm. Reason: Products do not meet length and diameter specifications..
- Recalling firm
- Arthrex, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-03-25
- Firm location
- Naples, FL, United States
Product description
K-Wire, 1.35 mm x 170 mm
Reason for recall
Products do not meet length and diameter specifications.
Data sourced from openFDA. This site is unofficial and independent of the FDA.