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[Recalled] VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the urinary tract. — There is the potential for holes in the clear sterile barrier of the device pou… | FDA 2024-07-

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductVTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the urinary tract.
Brand / manufacturerBoston Scientific Corporation
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-3151-2024
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date18 July 2024
EAN / barcode0871472904856

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Boston Scientific Corporation

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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