FDA Device recall Z-0146-2024
Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack
- FDA Device
- Class I
- ongoing
- Published 2023-11-01
On 2023-11-01 the FDA classified a Class I recall of Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack by Cardinal Health 200, citing demonstrated recognition and compatibility issues with syringe infusion pumps.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0146-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-09-20 |
| Published | 2023-11-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack
Reason
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Identifiers
| code_info | Product Code: 1180600777; UDI/DI: 10192253034608 - each, 20192253034605 - box, 50192253034606 - case; Lot Numbers:…Product Code: 1180600777; UDI/DI: 10192253034608 - each, 20192253034605 - box, 50192253034606 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206, 230207 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0146-2024%22
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