Molded Products recalled 26,900 MPC-130 See Luer Cap Sets used in intravascular administration nationwide in the United States. The recall is active as of 2026-04-15. The threaded sleeve may not engage and can detach. Health risk is high. Stop using the device and follow the manufacturer’s recall instructions.
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.
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
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The MPC-130 See Luer Cap Set is a medical device component used in intravascular administration. It is distributed nationwide.
If the sleeve does not engage, the connection could loosen, risking contamination or administration failure.
This recall is not part of a broader industry pattern.
Direct patient risk if used. Healthcare facilities may face replacement and inventory challenges.
FDA recall page Z-1774-2026 and manufacturer communications
Expect 4-6 weeks for replacement or refund depending on facility contracts
Keep recall letter, photos of labels, UDI and Lot numbers, and correspondence with Molded Products.
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.
No specific injuries were disclosed in the provided data. The FDA enforcement report lists a confirmed complaint about the engagement failure.
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