Medical Device Recall: MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A
MEDLINE INDUSTRIES, LP - Northfield · December 21, 2023
Reason for Recall
Medline 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.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
4320 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0965-2024
Status: ongoing
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