Quick Facts at a Glance
- Recall Date
- February 17, 2026
- Hazard Level
- HIGH
- Brand
- Molded Products
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL, PREGNANT, PETS
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Molded Products
- Product type
- Luer Cap Set
- Model numbers
- UDI +B144MPC1300/$$529105203895, Lot Number 20389
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 17, 2026
Reported by FDA DEVICE
April 15, 2026
RecallRadar source check
April 22, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Molded Products Inc or your healthcare provider for instructions. Notification method: Letter
About This Product
The MPC-130 See Luer Cap Set is a medical device component used in intravascular administration. It is distributed nationwide.
Why This Is Dangerous
If the sleeve does not engage, the connection could loosen, risking contamination or administration failure.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Direct patient risk if used. Healthcare facilities may face replacement and inventory challenges.
Practical Guidance
How to identify if yours is affected
- Check for UDI +B144MPC1300/$$529105203895 on the device label
- Check Lot Number 20389
- Verify product is MPC-130 See Luer Cap Set
Where to find product info
FDA recall page Z-1774-2026 and manufacturer communications
What timeline to expect
Expect 4-6 weeks for replacement or refund depending on facility contracts
If the manufacturer is unresponsive
- Escalate to hospital supply chain leadership
- File a report with FDA/CFB if manufacturer remains unresponsive
How to prevent similar issues
- Implement inbound inspection for sterile components
- Verify engagement mechanisms during QA
- Request verifications for future Luer cap sets
- Maintain proper inventory segregation for recalled lots
Documentation advice
Keep recall letter, photos of labels, UDI and Lot numbers, and correspondence with Molded Products.
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Product Details
Brand: Molded Products. Product: MPC-130 See Luer Cap Set. Model/UDI: UDI +B144MPC1300/$$529105203895, Lot Number 20389. Quantity: 26,900 units. Distribution: US nationwide in TN, TX, NV, IL, FL. Status: Active. Recall date: 2026-02-17.
Reported Incidents
No specific injuries were disclosed in the provided data. The FDA enforcement report lists a confirmed complaint about the engagement failure.
Key Facts
- Class II medical device recall
- High hazard level
- Threaded sleeve may not engage and detach
- Distributed nationwide in 5 states: TN, TX, NV, IL, FL
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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