Health & Personal Care
HIGH
FDA DEVICE
Molded Products MPC-130 See Luer Cap Set Recalled for High-Risk Assembly Issue (2026)
Molded Products recalled 26,900 MPC-130 See Luer Cap Sets used in intravascular administration nationwide in the United States. The recall is active as of 2026-04-15. The threaded sleeve may not engage and can detach. Health risk is high. Stop using the device and follow the manufacturer’s recall instructions.
Molded Products
Molded Products,