Smith & Nephew, Inc. DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener
Brand
Smith & Nephew, Inc.
Lot Codes / Batch Numbers
Batch 23GNX0077
Products Sold
Batch 23GNX0077
Smith & Nephew, Inc. is recalling DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener due to Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received ind. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contained K-WIRE .062X9 2PT DM wires instead of K-WIRE .045X9 2PT DM as described on the product label.
Recommended Action
Per FDA guidance
Smith & Nephew issued and Urgent Medical Device Recall Notice to its consignees on 07/09/2024 via overnight mail. The notice explained the problem, potential risk, and requested the return of the product. Sales representatives, District Offices, and/or Distributors were directed to notify their customers. For questions or concerns regarding this recall please contact FieldActions@smith-nephew.com.
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