See Luer Cap Set, MPC-130, set, administration, intravascular
Recall
- Recall Number
- Z-1774-2026
- Event Number
- 98469
- Firm
- Molded Products Inc
- FEI Number
- 1000138417
- Product Code
- FPA
- Status
- Open, Classified
- Root Cause
- Process control
- Initiated
- February 17, 2026
- Posted
- April 6, 2026
- Address
- 1812 Industrial Pkwy, Harlan, IA, 51537-2401
Description
See Luer Cap Set, MPC-130, set, administration, intravascular
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.
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 the contact noted below whether or not you have any of the impacted material so that Molded Products may acknowledge your receipt of this notification and process your return and credit. For complaints, adverse events, or questions, contact Teresa Wooster, [email protected]; Ph# 800-435-8957 ext. 236 Monday Friday 8:00am-4:30pm (CT), Fax# 800-227-7935.
US Nationwide distribution in the states of TN, TX, NV, IL, FL.
26900 units