FDAMarch 5, 2021device

MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then labeled and placed in carton with IFU. A closure strip, top and side labels are applied to the carton.

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

The hazard

The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

UPCs

8714729940289

Recall history

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

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