K-Wire recall
K-Wire, 1.35 mm x 170 mm
Why was K-Wire recalled?
Products do not meet length and diameter specifications.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084
- Product
- K-Wire, 1.35 mm x 170 mm
- Recalling firm
- Arthrex, Inc.
- Quantity
- 300 pieces
- Distribution
- Worldwide distribution - US Nationwide distribution in the states of OH, TN, MO, LA, IA, AZ, PA, NY, OR and the countries of to Belgium, Egypt, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Portugal, and Spain.
- Recall date
- May 11, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)