Recall Z-1774-2026— Molded Products Inc

Name: FDA recall Z-1774-2026
Creator: U.S. Food and Drug Administration
Published: 2026-02-17

Class II · Ongoing

Class II FDA medical device recall by Molded Products Inc, initiated 2026-02-17. It names one FDA 510(k) clearance: K925927. Product: See Luer Cap Set, MPC-130, set, administration, intravascular. Reason: 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..

Recalling firm: Molded Products Inc
Classification: Class II
Status: Ongoing
Initiated: 2026-02-17
Firm location: Harlan, IA, United States

510(k) clearances named in this recall

1 on FDA's record

K925927 — MPC-1000 INJECTION CAP/PLUGMolded Products, Inc.·cleared 1993-08-16

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

See Luer Cap Set, MPC-130, set, administration, intravascular

Reason for recall

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.