Recall Z-0486-2018 ยท FMI Needle, Hypodermic, Single Lumen
Arrow International Inc
Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial circulation or to other small vessels.
| Date | Jul 10, 2017 |
| Status | Terminated |
| Reason | Needle supplier indicated the presence of loose polypropylene foreign matter above release specification. |
| Root cause | Material/Component Contamination |
| Action | On July 10, 2017, Arrow International distributed Urgent Medical Device Recall notice and acknowledgment forms to customers. Customers are advised to take the following actions: 1. If you have affected stock, immediately discontinue use and quarantine any products listed in the notice, so that the affected products can be returned to Arrow. 2. To return product, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419- 8507, Attn: Customer Service or email to recalls@teleflex.com. This will allow us to document the amount of product you have on hand for return. A customer s |
| Distribution | ... |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K810675 | ARROW RADIAL ARTERY CATHETERIZATION SET Arrow Intl., Inc., Mar 27, 1981 |