See Luer Cap Set — Class II medical device recall Z-1774-2026
Ongoing recall by Molded Products Inc, reported 2026-04-15, distributed nationwide. Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based
| Recall number | Z-1774-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Molded Products Inc, Harlan, IA, United States |
| Recall initiated | 2026-02-17 |
| Classified | 2026-04-06 |
| Reported by FDA | 2026-04-15 |
| Distributed | Nationwide (US) |
| Quantity | 26,900 units |
| Lot numbers | 20389 |
Product
See Luer Cap Set, MPC-130, set, administration, intravascular
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1774-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.