Z-2039-2024 Class II
FDA device recall Z-2039-2024 was initiated by Mckesson Medical-Surgical Inc. Corporate Office on Apr 23, 2024 and is designated Class II. Reason for recall: Quarantined product was inadvertently distributed Affected quantity: 5 Boxes (20 per box, 100 eaches).
Recall Details
- Product Type
- Devices
- Report Date
- Jun 19, 2024
- Initiation Date
- Apr 23, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 Boxes (20 per box, 100 eaches)
Product Description
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 for Recall
Quarantined product was inadvertently distributed
Distribution Pattern
US Nationwide distribution in the state of NJ.
Code Information
UDI-DI: 20884521012230 Lot Code: 330737X
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2039-2024
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026