The Recall Desk

Manufacturer

Molded Products Inc

4 recalls in our database name Molded Products Inc as the manufacturing or recalling firm.

What the numbers show

Total
4
Critical
0
Severe
0
Most recent
2026-04-15

Of the 4 recalls from Molded Products Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–4 of 4

  • HighFDA (Devices)·Z-1774-2026·2026-04-15

    Molded Products Luer cap sets recalled after threaded sleeve detachment complaint

    Molded Products is recalling the MPC-130 See Luer Cap Set following a confirmed complaint that the threaded sleeve was not engaged and became detached. 26,900 units are affected.

    Product
    See Luer Cap Set, MPC-130, set, administration, intravascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2354-2019·2019-08-28

    Molded Products Recalls Mislabelled Luer Lock Sets for IV Administration

    Molded Products Inc is recalling 130,000 Luer Lock Sets (Catalog # MPC-125) because some packages were incorrectly labeled as a different product.

    Product
    Luer Lock Set - Catalog # MPC-125, for IV administration sets.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1679-2017·2017-04-05

    Molded Products Recalls Non-Sterile Hemodialysis Tubing Connectors

    Molded Products Inc is recalling 400 non-sterile hemodialysis tubing connectors due to a reported leak. The product was distributed to Ontario, Canada.

    Product
    Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0969-2013·2013-03-27

    Molded Products Recalls Sterile Hemodialysis Line Sets Due to Leaks

    Molded Products Inc is recalling 1,200 sterile access and return line sets used in hemodialysis because they leak at the connection site.

    Product
    Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing.
    Category
    Medical Device
    Distribution
    1 state