Recall Z-1344-2016
AngioDynamics Inc. · initiated November 3, 2015
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
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 in the vessel, and is then removed before sliding the catheter over the guidewire
Codes / lots: Batch/Lot No. 4925152, 4930012; Use By 2018-08
Reason for recall
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".
FDA-determined cause: Process control
Action taken
On November 03, 2015, Navilyst Medical distributed Urgent Voluntary Medical Device Recall notices to their customers via courier service. Customers were advised to immediately remove the recall product from inventory and to segregate the products in a secure location for return to AngioDynamics, Inc. Customers should immediately forward a copy of the recall notification letter to all sites if these products were further distributed. If affected product is located in your institution, please call AngioDynamics, Inc. Customer Service at 1-800-772-6446 between 8:00 a.m. and 7:00 p.m. (Monday - Friday EST) to obtain a replacement or credit for your returned product. Promptly complete, sign and return the enclosed Reply Verification Tracking Form (even if you do not have any product to return). The Reply Verification Tracking form can be submitted via fax to: Attn: Convenience Kits - Procedure Products Needles 1-800-782-1357 or via email to rdenino@angiodynamics.com or sbaxter@angiodynamics.com.
Details
- Recall number
- Z-1344-2016
- Initiated
- November 3, 2015
- Posted by FDA
- April 7, 2016
- Terminated
- March 16, 2017
- Product code
- OEZ – Cardiovascular Procedure Kit
- Quantity
- 100 kits
- Distribution
- US Nationwide in the states of CA, IL, MA, SC, TX
- Recalling firm
- AngioDynamics Inc., Glens Falls, NY
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-1343-2016 Class II | NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 651919311…Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended… | 11/03/2015Terminated |
| Z-1345-2016 Class II | NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No. 60080094…Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended… | 11/03/2015Terminated |
| Z-1346-2016 Class II | NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN…Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended… | 11/03/2015Terminated |