Recalling firm
Molded Products Inc
Product type
Device
Status
Ongoing
Report date
2026-04-15
Distribution
US Nationwide distribution in the states of TN, TX, NV, IL, FL.
Firm state
IA
Product quantity
26900 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason 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.
Product description
See Luer Cap Set, MPC-130, set, administration, intravascular
Code / lot info
UDI +B144MPC1300/$$529105203895, Lot Number 20389
Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.