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FDADecember 13, 2023device

Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Express chest drains are pre-packaged with sterile water syringes which have bene recalled. If the device is not kept in an upright position, the patient may be exposed to infectious material. Subsequent hazards include but are not limited to infection, abscess, sepsis, and death.

What to do

FDA enforcement status: Ongoing

Brands named

maquet cardiovascularmaquet

UPCs

00650862115147

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit — Recall Details · AllClear