FDA Recall Open, Classified

McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)

Recall: Z-2940-2024 · Initiated July 24, 2024

Recall

Recall Number
Z-2940-2024
Event Number
95041
Firm
Cypress Medical Products LLC
FEI Number
1451040
Product Code
FMF
Status
Open, Classified
Root Cause
Other
Initiated
July 24, 2024
Posted
August 29, 2024
Address
9954 Mayland Dr, Richmond, VA, 23233-1464

Description

McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)

Reason

Affected syringes lack FDA clearance.

Action

On July 24, 2024, the firm issued Urgent Medical Device Recall letters to affected customers. Consignees were advised that the affected syringes lack FDA clearance. Customers should immediately quarantine and discontinue use of any affected product. Recalled product should be destroyed on location. If you have further distributed the product, please notify your downstream accounts of the recall. For questions about this notification please contact [email protected].

Distribution

US distribution only. Domestic distribution nationwide.

Quantity

24,693,200 eaches (US)