FDAJuly 18, 2024device

Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To provide external drainage of the urinary tract.

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

The hazard

There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

0871472932337

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To provide external drainage of the urinary tract. — Recall Details · AllClear