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Recall Observatory FDA recall evidence

Device product

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

Z-1345-2016

November 03, 2015

Class II

Product summary

Firm
AngioDynamics Inc.
Event
Event 72957
Status
Terminated
Classification
Class II
Quantity
8 kits
Official record key
device-enforcement:Z-1345-2016

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/Lo. 4925662 Use By 2017-02

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".