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Recall Observatory FDA recall evidence

Device product

NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN Product No. H7496013198101 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.

Z-1346-2016

November 03, 2015

Class II

Product summary

Firm
AngioDynamics Inc.
Event
Event 72957
Status
Terminated
Classification
Class II
Quantity
45 kits
Official record key
device-enforcement:Z-1346-2016

Official wording

Reason: 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".

Code information: Batch/Lot No. 4931728, 4933094; Use By 2017-03

Distribution pattern: US Nationwide in the states of CA, IL, MA, SC, TX

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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".