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Open, Classified

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

FDA Recall Z-2940-2024 · Posted 2024-08-29

Recall StatusOpen, Classified
Product CodeFMF
Date Initiated2024-07-24
Product Quantity24,693,200 eaches (US)

Reason for Recall

Affected syringes lack FDA clearance.

Firm 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].

Root Cause

Other

Distribution Pattern

US distribution only. Domestic distribution nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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