Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product… — Class II medical device recall Z-1408-2013
Terminated recall by Merit Medical Systems, Inc., reported 2013-06-05, distributed nationwide. Merit Medical Systems is recalling various lots of Performa Cardiac Multipacks containing a JR4.0 catheter due
| Recall number | Z-1408-2013 |
|---|---|
| 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 | 2013-05-02 |
| Classified | 2013-05-25 |
| Reported by FDA | 2013-06-05 |
| Terminated | 2013-07-22 |
| Distributed | Nationwide (US) |
| Quantity | 1,465 |
| Lot numbers | 1662385, 1662386, 1662387, 1662390, 1662391 |
Product
Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage: Angiographic catheters are designed to be used for delivering radiopaque media to selected sites in the vascular system in conjunction with routine diagnostic procedures.
Reason for recall
Merit Medical Systems is recalling various lots of Performa Cardiac Multipacks containing a JR4.0 catheter due to 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-1408-2013. 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.