Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
Check against the official notice below — it lists the full affected range.
Stryker GmbH is recalling 17 units of Femoral Nail, A/R T2 Femur 10x340 mm (Product Number 18251034S, Lot code K0957B1) distributed to Alabama, Colorado, Florida, Kentucky, North Carolina, Tennessee, Utah, and Washington. The manufacturer discovered that some products may not meet specifications due to improper cannulation of the nails, which could reduce component strength and lead to premature nail breakage.
The recall record does not specify a remedy or recommended action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
Reason for recall: The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage. Distribution: The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA. Quantity: 17 Lot/code info: GTIN 04546540199508; Lot code: K0957B1
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.