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FDA (Device enforcement)Recalled 2023-05-18class ii

Maquet Medical Systems USA: BEQ-HMO 50000-USA/ QUADROX-i Small, Oxygenator used during cardiopulmonary bypass Item no. 701067905

Hazard

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

Details from the source

Reason for recall: 1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia. Distribution: Domestic distribution nationwide. Quantity: 1,784 (US) Lot/code info: UDI-DI: 04058863019079 All lots

UPC codes

04058863019079

Source

Official record: FDA (Device enforcement)

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

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