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Open, Classified

24 BLOOD CULTURE KIT, REF DYNDH1632

FDA Recall Z-0313-2024 · Posted 2023-11-16

Recalling FirmMEDLINE INDUSTRIES, LP - Northfield
Recall StatusOpen, Classified
Product CodeGJE
Date Initiated2023-11-01
Product Quantity3160 kits

Reason for Recall

This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.

Firm Action

Medline Industries issued a MEDICAL DEVICE RECALL notice to its consignees on 11/01/2023 via email. The notice explained the issue and requested that the destruction of the affected kits. Consignees were also instructed to notify all parties if the kits were transferred.

Root Cause

Under Investigation by firm

Distribution Pattern

US Nationwide distribution in the state of California.

Official Source

View FDA Recall →

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

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