FDADecember 21, 2023device

MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

4019532713420510195327134204

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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