FDA-Device2026-04-15Class IIPROCESSING DEFECT
Molded Products MPC-130 See Luer Cap Set recalled for detachment risk
What this means
Molded Products Inc. is recalling the MPC-130 See Luer Cap Set used in medical IV administration. The threaded sleeve can fail to engage properly, causing the cap to become detached during use. This affects 26,900 units distributed across Tennessee, Texas, Nevada, Illinois, and Florida.
- Stop using any MPC-130 See Luer Cap Set immediately
- Check your inventory for Lot Number 20389 or UDI +B144MPC1300/$$529105203895
- Contact Molded Products Inc. for instructions on return or replacement
- Review affected patient records and assess any potential complications
The agency's original wording
Hazard
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.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution in the states of TN, TX, NV, IL, FL.
Affected count
26900 units
Manufactured in
1812 Industrial Pkwy, Harlan, IA, United States
Products
See Luer Cap Set, MPC-130, set, administration, intravascular
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1774-2026Want us to check the next one for you?
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