Merit Medical Performa Angiographic Catheter 5F Multipack — Class II medical device recall Z-0045-2014
Terminated recall by Merit Medical Systems, Inc., reported 2013-10-30, distributed in CO, MS, VA. 4 lots of Performa Cardiac Multipacks contain a JR4.0 catheter with a slight variation in tip shape.
| Recall number | Z-0045-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merit Medical Systems, Inc., South Jordan, UT, United States |
| Recall initiated | 2013-09-13 |
| Classified | 2013-10-22 |
| Reported by FDA | 2013-10-30 |
| Terminated | 2014-01-03 |
| Distributed | CO, MS, VA |
| Quantity | 200 |
| Lot numbers | 7560-43/I663860, 7560-43/I663861, 7560-G3/I664519, 7560-G3/I666388 |
| Model numbers | 7560-43, 7560-G3 |
Product
Merit Medical Performa Angiographic Catheter 5F Multipack. Part numbers 7560-43 and 7560-G3.
Reason for recall
4 lots of Performa Cardiac Multipacks contain a JR4.0 catheter with a slight variation in tip shape.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0045-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.