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FDAFebruary 7, 2022device

PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog Number: 8713030U

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

The hazard

Units not properly inspected prior to release to the market, may not function as indicated in the product labeling, resulting in syringe detection and infusion accuracy that can result in delays in therapy, overinfusion, or underinfusion.

What to do

FDA enforcement status: Terminated

Brands named

b braun medical

UPCs

04046963716745

Recall history

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

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