Boston Scientific Corporation recalls Flexima Regular Kit Nephrostomy Catheter System Kit, Materia
Recalled Product
Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To provide external drainage of the urinary tract.
Hazard / Issue
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
Issued by
FDA
Distribution: US, Colombia, Philippines, Russia
Lot/Code Info: GTIN/UDI 0871472932337, Lot # 33550953, exp. 03/04/2027
View official government recall
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