FDA Enforcement
Class II
Terminated
NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 651919311, UPN Product No. H7496519193111 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
Recall: Z-1343-2016
·
Reported April 13, 2016
Enforcement
- Recall Number
- Z-1343-2016
- Event ID
- 72957
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- AngioDynamics Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- April 13, 2016
- Initiation Date
- November 3, 2015
- Classification Date
- April 7, 2016
- Termination Date
- March 16, 2017
- Address
- 10 Glens Falls Tech Park, N/A, Glens Falls, NY, 12801-3864, United States
Description
NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 651919311, UPN Product No. H7496519193111 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
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 Info
Batch/Lot No. 4921353 Use By 2018-05 and Batch/Lot No. 4932710 Use By 2018-06-30
Distribution
US Nationwide in the states of CA, IL, MA, SC, TX
Quantity
136 kits