Medline recalls specific adult blood culture trays due to expired Bactec components not listed on kit inserts. Users must check expiration dates to avoid potential risks from outdated materials.
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.
Medline is recalling adult blood culture trays that may contain expired Bact:ec components. This could lead to inaccurate test results if the user doesn't verify the expiration date on the Bactec component inside the kit.
The recall is due to expired Bactec components not being listed on the kit inserts. If users don't check the expiration date of the Bactec inside the kit, they might use outdated materials that could cause inaccurate test results.
Healthcare professionals using Medline adult blood culture trays with specific reorder numbers and lot numbers are affected. Patients receiving blood tests using these kits may be at risk if the components are expired.
Check for the reorder number DYNDH1194A and lot number 23JBO540 on the blood culture tray. The product has a unique identifier (UDI/DI) of 40195327432301 for the case and 10195327432300 for the unit.
Inspect the Bactec component inside the kit for its expiration date to ensure it is current.
Medline is recalling specific adult blood culture trays because they may contain expired Bactec components not listed on the kit inserts.
Look for the reorder number DYNDH1194A and lot number 23JBO540 on the blood culture tray, with UDI/DI numbers 40195327432301 (case) and 10195327432300 (unit).
Check the expiration date on the Bactec component inside the kit to ensure it is current; no action is needed if it is valid.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0969-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-0969-2024 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
