DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener
Reported: September 25, 2024 Initiated: July 9, 2024 #Z-3171-2024
Product Description
DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener
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.
Details
- Recalling Firm
- Smith & Nephew, Inc.
- Units Affected
- 24 units
- Distribution
- US, Canada, Norway
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener. Recalled by Smith & Nephew, Inc.. Units affected: 24 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 25, 2024. Severity: Moderate. Recall number: Z-3171-2024.
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