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FDA (Device enforcement)Recalled 2023-05-02class ii

Smith & Nephew, Inc.: Smith&Nephew ENGAGE Cementless Partial Knee System, Tibial Anchor Stem, Part Numbers: a) REF 1-10011-100 (SIZE 1-2), b) REF 1-10011-200 (SIZE 3-4), c) REF 1-10011-300 (SIZE 5-6);

Hazard

Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision.

Details from the source

Reason for recall: Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision. Distribution: US Nationwide distribution. Quantity: 1596 units Lot/code info: a) REF 1-10011-100, UDI/DI 00885556873083; b) REF 1-10011-200, UDI/DI 00885556873090; c) REF 1-10011-300, UDI/DI 00885556873106; ALL BATCHES

UPC codes

00885556873083, 00885556873090, 00885556873106

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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