Arthrex, Inc. K-Wire, 1.35 mm x 170 mm Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
K-Wire, 1.35 mm x 170 mm
Brand
Arthrex, Inc.
Lot Codes / Batch Numbers
Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084
Products Sold
Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084
Arthrex, Inc. is recalling K-Wire, 1.35 mm x 170 mm due to Products do not meet length and diameter specifications.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Products do not meet length and diameter specifications.
Recommended Action
Per FDA guidance
The firm sent a recall notification to the consignees on 03/25/2022 via email. The consignees were instructed to discontinue use, sale, and distribution of the product. The consignees were also instructed to contact FLS@arthrex.com to arrange return of the affected product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026