Official recall notice

FDA DeviceClass IINotable

FDA Recall: See Luer Cap Set, MPC-130, set, administration, intravascular

Recall date
2026-04-15
FDA class
Class II

Why it was recalled

Hazard

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.

Recommended action

What to do

26900 units

Product description

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.

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