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

Maquet Medical Systems USA: QUADROX-i Small Adult, Oxygenator used during cardiopulmonary bypass Model Item no. HMO 50000-USA 701067891 HMO 51000-USA 701067895

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: 0 (US) Lot/code info: Model Item no. UDI-DI HMO 50000-USA 701067891 4058863019055 HMO 51000-USA 701067895 4058863019185 All lots

UPC codes

4058863019055, 4058863019185

Source

Official record: FDA (Device enforcement)

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

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