Recall Z-2039-2024— Mckesson Medical-Surgical Inc. Corporate Office
Class II · Completed
Class II FDA medical device recall by Mckesson Medical-Surgical Inc. Corporate Office, initiated 2024-04-23. It names one FDA 510(k) clearance: K131641. 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.
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office
- Classification
- Class II
- Status
- Completed
- Initiated
- 2024-04-23
- Firm location
- Richmond, VA, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.