RegWardenFDA facility compliance records
Company

MOLDED PRODUCTS INC.

4 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2012: 1 recalls; 2015: 1 recalls; 2019: 1 recalls; 2026: 1 recalls1’12’13’141’15’16’17’181’19’20’21’22’23’24’251’26
  • Recalls (4)

Registered facilities (1)

Recalls & enforcement

  • Class IIOngoing2026-02-17
    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.
  • Class IITerminated2019-06-10
    Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.
  • Class IITerminated2015-01-20
    A customer relayed a complaint of a leaking dialysis tubing connector.
  • Class IITerminated2012-06-19
    The recalled product leaks at the connection site.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “MOLDED PRODUCTS INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9007334-molded-products-inc/

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