FDA recall Z-2354-2019

Molded Products Inc · Class II · device

Product

Luer Lock Set - Catalog # MPC-125, for IV administration sets.

Reason for recall

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.

Distribution

Distribution US nationwide.

Key facts

Status
Terminated
Initiation date
2019-06-10
Report date
2019-08-28
Termination date
2021-05-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Harlan, IA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2354-2019