Molded Products Inc recalls See Luer Cap Set
- Recalling company
- Molded Products Inc
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 17, 2026
- Reported
- Apr 15, 2026
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Status
- Ongoing
- Quantity
- 26900 units
- Lot / codes
- UDI +B144MPC1300/$$529105203895, Lot Number 20389
- Company location
- Harlan, IA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1774-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1774-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.