FDA recall record

Boston Scientific Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF recall — FDA Z-3149-2024

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

Class IIclassification
Z-3149-2024official record ID
Sep 25, 2024report date

Recall record at a glance

Official recordZ-3149-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBoston Scientific Corporation
Report dateSep 25, 2024
Recall initiation dateJul 18, 2024
Quantity10 units
LocationMaple Grove, MN, United States

Official product description

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

Why the product was recalled

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

Distribution information

US, Colombia, Philippines, Russia

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.