Class II
Medical Device Recall: DIAMOND POINT, BOTH ENDS K-WIRE, REF 128062, metallic bone fixation fastener
Smith & Nephew, Inc. · July 9, 2024
Reason for Recall
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.
Distribution
US, Canada, Norway
Quantity Affected
73 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3172-2024
Status: ongoing
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