—#204218

Product

24 BLOOD CULTURE KIT, REF DYNDH1632

FDA product code: GJE — Tray, Blood Collection
Device class: Class 2
Medical specialty: Clinical Chemistry
Affected lot / code info: UDI/DI 40193489916141 (case), 10193489916140 (unit): Lot Numbers: 23EMF710, 23DMF154, 23DMA779

Why it was recalled

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

Root cause (FDA determination)

Under Investigation by firm

Action the firm took

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.

Recalling firm

Firm: MEDLINE INDUSTRIES, LP Northfield
Address: 3 Lakes Dr, Northfield, Illinois 60093-2753

Distribution

Distribution pattern: US Nationwide distribution in the state of California.

Timeline

Recall initiated: 2023-11-01
Posted by FDA: 2023-11-16
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #204218. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.