Class II

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

Molded Products Inc · February 17, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

26900 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1774-2026

Status: ongoing

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