Recall Z-1774-2026 ยท FPA Set, Administration, Intravascular
Molded Products Inc
See Luer Cap Set, MPC-130, set, administration, intravascular
| Date | Apr 6, 2026 (initiated Feb 17, 2026) |
| Status | Open, Classified |
| 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. |
| Root cause | Process control |
| Action | Molded Products, Inc. issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 02/17/2026 via USPS First Class Mail. The notice explained the issue and requested the following: Please take the following actions: 1. Please inspect your inventory to determine if you have any of the affected lot. Quarantine the affected product and initiate a return to Molded Products, Inc. for credit. 2. Share this recall notification will all users of the product to ensure they are also aware of this recall. 3. Complete the attached Medical Device Recall Customer Response Form and return to |
| Quantity | 26900 units |
| Distribution | US Nationwide distribution in the states of TN, TX, NV, IL, FL. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K925927 | MPC-1000 INJECTION CAP/PLUG Molded Products, Inc., Aug 16, 1993 |