Recall Z-2940-2024— Cypress Medical Products LLC

Name: FDA recall Z-2940-2024
Creator: U.S. Food and Drug Administration
Published: 2024-07-24

Class II · Ongoing

Class II FDA medical device recall by Cypress Medical Products LLC, initiated 2024-07-24. It names one FDA 510(k) clearance: K103830. Product: 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..

Recalling firm: Cypress Medical Products LLC
Classification: Class II
Status: Ongoing
Initiated: 2024-07-24
Firm location: Richmond, VA, United States

510(k) clearances named in this recall

1 on FDA's record

K103830 — JIANGSU SHENLI MEDICAL PRODUCTION CO. LTD. PISTON SYRINGE (5CC LUER LOCK)Jiangsu Shenli Medical Production Factory·cleared 2011-07-29

K-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

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

Reason for recall

Affected syringes lack FDA clearance.

Data sourced from openFDA. This site is unofficial and independent of the FDA.