Medical Device Recall: MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723
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
960 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0967-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.