Molded Products, Inc.
Molded Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2002, with 4 FDA device recalls on record.
Top product codes for Molded Products, Inc.
FDA recalls by Molded Products, Inc.
- Z-1774-2026 — See Luer Cap Set, MPC-130, set, administration, intravascular
- Z-2354-2019 — Luer Lock Set - Catalog # MPC-125, for IV administration sets.
- Z-1679-2017 — Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
- Z-0969-2013 — Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Molded Products, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.