RecallRadar

FDA Device recall Z-2742-2018

1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body

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

AgencyFDA Device
Recall numberZ-2742-2018
ClassificationClass II
Statusterminated
Initiated2018-02-02
Published2018-08-22
Last updated2026-09-13 11:54 UTC
CompanyMerit Medical Systems
DistributionUS

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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.