- Recalling firm
- Molded Products Inc
- 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.
- Affected products (lot / model / serial)
- UDI +B144MPC1300/$529105203895, Lot Number 20389
- Units affected
- 26900 units
- Distribution pattern
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Firm location
- Harlan, IA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1774-2026
- Recall initiated
- February 17, 2026
- FDA classification date
- April 6, 2026
- FDA report date
- April 15, 2026
- FDA event ID
- 98469
- Last updated on HTM Vibe
- July 24, 2026