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Recall Observatory FDA recall evidence

Device product

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

Z-1774-2026

February 17, 2026

Class II

Product summary

Firm
Molded Products Inc
Event
Event 98469
Status
Ongoing
Classification
Class II
Quantity
26900 units
Official record key
device-enforcement:Z-1774-2026

Official wording

Reason: 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.

Code information: UDI +B144MPC1300/$$529105203895, Lot Number 20389

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.