FDA Device recall Z-2039-2024
Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal…
- FDA Device
- Class II
- completed
- Published 2024-06-19
On 2024-06-19 the FDA classified a Class II recall of Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal… by Mckesson Medical Surgical Corporate Office, citing quarantined product was inadvertently distributed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2039-2024 |
| Classification | Class II |
| Status | completed |
| Initiated | 2024-04-23 |
| Published | 2024-06-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Mckesson Medical Surgical Corporate Office |
| Distribution | US |
Product
Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal Catalog Number: 8881560125
Reason
Quarantined product was inadvertently distributed
Identifiers
| code_info | UDI-DI: 20884521012230 Lot Code: 330737X |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: completed.
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All Mckesson Medical Surgical Corporate Office recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2039-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.