MOLDED PRODUCTS INC.
4 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (4)
- Inspections (3)
Devices registered here (1)
- Forceps, General & Plastic SurgeryProduct code GEN (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800
Recalls & enforcement
- Class IIOngoing2026-02-17Molded 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 IITerminated2019-06-10Mislabeling - 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 IITerminated2015-01-20A customer relayed a complaint of a leaking dialysis tubing connector.
- Class IITerminated2012-06-19The recalled product leaks at the connection site.
FDA inspections (3)
- NAI2022-10-07No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- NAI2018-04-11No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- NAI2017-03-10No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “MOLDED PRODUCTS INC. (FEI 1000138417) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000138417-molded-products-inc/
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