Merit Maestro Microcatheter — Class II medical device recall Z-0162-2015
Terminated recall by Merit Medical Systems, Inc., reported 2014-11-12, distributed nationwide. These microcatheters were packaged with a 2.8 F distal tip, rather than the labeled 2.4 F.
| Recall number | Z-0162-2015 |
|---|---|
| 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 | 2014-09-26 |
| Classified | 2014-10-31 |
| Reported by FDA | 2014-11-12 |
| Terminated | 2014-11-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | IN |
| Quantity | 56 units |
| Reason classes | labeling |
| Lot numbers | 2017, H665694, H665696, H669824 |
| Model numbers | 28MC24130ST, 28MC24150SN |
| Expiration dates | 2014-07-31 |
Product
Merit Maestro Microcatheter, 2.4F 130cm Straight, REF28MC24130ST, Rx Only, Non-pyrogenic Sterile if package is unopened or undamaged.
Reason for recall
These microcatheters were packaged with a 2.8 F distal tip, rather than the labeled 2.4 F.
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-0162-2015. 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.