See Luer Cap Set, MPC-130, set, administration… recallZ-1774-2026 · Molded Products Inc · initiated Feb 17, 2026
Class II Open, Classified All recalls posted in April 2026
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Molded Products Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Process control
What the company is doing
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.
Recall details
- Recall number
- Z-1774-2026
- Recall class
- Class II
- Status
- Open, Classified
- Initiated by the company
- Feb 17, 2026
- Posted by the FDA
- Apr 6, 2026
- Recalling firm
- Molded Products Inc
- Quantity
- 26900 units
- Product code
- FPA
- FDA submissions
- K925927
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
Product description
See Luer Cap Set, MPC-130, set, administration, intravascular
Code information (models, lots, serial numbers)
UDI +B144MPC1300/$$529105203895, Lot Number 20389
Other devices under the same FDA submission
1 device cleared under K925927 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Molded Products, Inc. MPC-130Molded Products, Inc. · Set, Administration, Intravascular2 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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