FDA recall Z-1774-2026

Product

See Luer Cap Set, MPC-130, set, administration, intravascular

Reason for recall

Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.

Distribution

US Nationwide distribution in the states of TN, TX, NV, IL, FL.

Key facts

Status

Ongoing

Initiation date

2026-02-17

Report date

2026-04-15

Voluntary/Mandated

Voluntary: Firm initiated

Location

Harlan, IA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1774-2026