Recall Z-2940-2024

Cypress Medical Products LLC · initiated July 24, 2024

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

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

Codes / lots: All lots of the affected product 102-S60C, SYRINGE, LL 60CC which are within their expiration date, are being recalled. Products were manufactured within the last five years. Affected lots: All lots beginning with alpha characters CLN. UDI-DI (01)30612479170316

Reason for recall

Affected syringes lack FDA clearance.

FDA-determined cause: Other

Action taken

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 productcomplaint@McKesson.com.

Details

Recall number
Z-2940-2024
Initiated
July 24, 2024
Posted by FDA
August 29, 2024
Product code
FMF – Syringe, Piston
Quantity
24,693,200 eaches (US)
Distribution
US distribution only. Domestic distribution nationwide.
Recalling firm
Cypress Medical Products LLC, Richmond, VA

Official FDA recall record