FDANovember 3, 2015device

NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER, REF Catalog No. 65230029, UPN Product No. H965652300290, Product is packed as a box of 30 pieces, box label contains UPN Product No. H965652300291 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening i...

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

The hazard

Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended specification. Specifically, at least a portion of the affected lot is unable to accept a 0.038" guidewire as intended. In some cases the inner lumen was found to be 0.036".

What to do

FDA enforcement status: Terminated

Brands named

angiodynamics

Recall history

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

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