FDA Device recall Z-1774-2026
See Luer Cap Set, MPC-130, set, administration, intravascular
- FDA Device
- Class II
- ongoing
- Published 2026-04-15
On 2026-04-15 the FDA classified a Class II recall of See Luer Cap Set, MPC-130, set, administration, intravascular by Molded Products, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1774-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-17 |
| Published | 2026-04-15 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Molded Products |
| Distribution | US |
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.
Identifiers
| code_info | UDI +B144MPC1300/$$529105203895, Lot Number 20389 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1774-2026%22
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