Molded Products Inc: Set, Administration, Intravascular
Molded Products Inc is recalling the MPC-130 See Luer Cap Set, a medical device used for intravenous administration, because the threaded sleeve can become detached. The recall affects units distributed nationwide, primarily in Tennessee, Texas, Nevada, Illinois, and Florida. This is a Class II recall, meaning the product could cause serious health problems or failure.
- Recalling firm
- Molded Products Inc
- Product
- See Luer Cap Set, MPC-130, set, administration, intravascular
- 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-02-17
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/8a547b01-8028-481e-9a4e-dd2368e16478