FDA-Device2024-02-07Class II
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723
MEDLINE INDUSTRIES, LP - Northfield
Hazard
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.
Sold states
US Nationwide distribution.
Affected count
960 units
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0967-2024Don't want to check this manually?
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