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Medical Device

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

Recall date: 2026-04-15 · Source: FDA_DEVICE
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.
Units affected
26900 units
Description
See Luer Cap Set, MPC-130, set, administration, intravascular
View official recall notice →