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MEDLINE INDUSTRIES, LP – Northfield Recall 93731

Description: MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C

MEDLINE INDUSTRIES, LP – Northfield Recall 93731 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-0968-2024
Event ID93731
Event DescriptionMEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C
Product TypeDevices
DistributionUS Nationwide distribution.
Quantity4200 units
Recall ReasonMedline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Device Classification20240207
Device Code InfoUDI/DI 40195327509874 (case), 10195327509873 (unit), Lot Numbers: 23JBQ525
Center Classification Date20240201
Recall Initiation Date20231221
Recalling FirmMEDLINE INDUSTRIES, LP - Northfield
Initial Notification Letter
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