FDA Device recall Z-2354-2019
Luer Lock Set - Catalog # MPC-125, for IV administration sets
- FDA Device
- Class II
- terminated
- Published 2019-08-28
On 2019-08-28 the FDA classified a Class II recall of Luer Lock Set - Catalog # MPC-125, for IV administration sets by Molded Products, citing mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2354-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-10 |
| Published | 2019-08-28 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Molded Products |
| Distribution | US |
Product
Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Reason
Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.
Identifiers
| code_info | LOT NUMBER: 20266 UDI # +B144MPC1251/$$52232420266N Expiration Date 11/20/2022 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2354-2019%22
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