FDANovember 3, 2015device

NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No. 60080094, UPN Product No. H749600800941 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter over the guidewire

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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