Official recall record
MEDLINE BLOOD CULTURE BOTTLE KIT, Reorder Number DYNDH1738A
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-12-21
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 40195327239849
- Brand on record
- MEDLINE INDUSTRIES, LP - Northfield
- Product category
- Medical Device
What the authority reported
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
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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