Molded Products Inc: See Luer Cap Set, MPC-130, set, administration, intravascular
Read the official notice at FDA (device) →
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Molded Products Inc
- Product
- See Luer Cap Set, MPC-130, set, administration, intravascular
- Reason / 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.
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Recall initiated
- 2026-02-17
- Code info
- UDI +B144MPC1300/$$529105203895, Lot Number 20389
- Product quantity
- 26900 units
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Harlan
- State
- IA
- Country
- United States
- Event id
- 98469
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