FDA Device recall Z-2742-2018
1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body
- FDA Device
- Class II
- terminated
- Published 2018-08-22
On 2018-08-22 the FDA classified a Class II recall of 1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body by Merit Medical Systems, citing supplier manufacturing defect with the syringe plunger tip.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2742-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-02 |
| Published | 2018-08-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Merit Medical Systems |
| Distribution | US |
Product
1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.
Reason
Supplier manufacturing defect with the syringe plunger tip.
Identifiers
| code_info | Catalog Number: Lot Number: K01-05526P H1258821, K01-07427 H1263015, K0…Catalog Number: Lot Number: K01-05526P H1258821, K01-07427 H1263015, K01-07477P H1250809 and H1242962, K01-07930P H1246733, MSS011-DG H1246809, K02-00565C H1258361, MSS011-LG H1246810, K02-01260B H1258575 and H1265248, MSS011-PR H1242752, MSS011-R H1242754 and H1255507, K02-01331A H1252652, K04-00748 H1258488 and H1264381, MSS011-Y H1246811, MSS011-YP H1242927, K12-03636 H1258530, and MSS011 H1242750, H1246807 and H1255504. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2742-2018%22
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