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FDA (Device enforcement)Recalled 2024-10-02class ii

Smith & Nephew Inc: smith&nephew GENESIS II NONPOROUS POSTERIOR STABILIZED FEMORAL COMPONENT, SIZE 5 LEFT, REF 71421015; Uncoated knee femur prosthesis, metallic

Hazard

Complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 5N RIGHT implant instead of a GENESIS II POSTERIOR STABILIZED FEMORAL SIZE 5 LEFT as described on the product label.

Details from the source

Reason for recall: Complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 5N RIGHT implant instead of a GENESIS II POSTERIOR STABILIZED FEMORAL SIZE 5 LEFT as described on the product label. Distribution: US Distribution to states of: MS, TN, NC, CA, GA, DE, AL, and OUS distribution to country of: Canada Quantity: 5 units Lot/code info: UDI/DI 03596010469212, Batch number 23LM02331

UPC codes

03596010469212

Source

Official record: FDA (Device enforcement)

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

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