Boston Scientific Corporation recalls Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To provide external drainage of th

Recalled September 25, 2024 · FDA recall Z-3149-2024 · Boston Scientific

Hazard

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

Units

10 units

Sold at

US, Colombia, Philippines, Russia

Description

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

Product

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

Manufacturer(s)

Boston Scientific Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →