FDA Device recall Z-0045-2014
Merit Medical Performa Angiographic Catheter 5F Multipack
- FDA Device
- Class II
- terminated
- Published 2013-10-30
On 2013-10-30 the FDA classified a Class II recall of Merit Medical Performa Angiographic Catheter 5F Multipack by Merit Medical Systems, citing 4 lots of Performa Cardiac Multipacks contain a JR4.0 catheter with a slight variation in tip shape.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0045-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-13 |
| Published | 2013-10-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Merit Medical Systems |
| Distribution | CO, MS, VA |
Product
Merit Medical Performa Angiographic Catheter 5F Multipack. Part numbers 7560-43 and 7560-G3.
Reason
4 lots of Performa Cardiac Multipacks contain a JR4.0 catheter with a slight variation in tip shape.
Identifiers
| code_info | Part Number/Lot Number: 7560-43/I663860, 7560-43/I663861, 7560-G3/I664519 and 7560-G3/I666388. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0045-2014%22
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