See Luer Cap Set recall
See Luer Cap Set, MPC-130, set, administration, intravascular
Why was See Luer Cap Set 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI +B144MPC1300/$$529105203895, Lot Number 20389
- Product
- See Luer Cap Set, MPC-130, set, administration, intravascular
- Recalling firm
- Molded Products Inc
- Quantity
- 26900 units
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Recall date
- April 15, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)