Medline Industries recalls Centurion Silver Antimicrobial VAD Drive (ref DT18760) due to expired component. Affected units have UDI/DI 10653160274841 and lot numbers 22ABO498. No specific action steps provided in recall notice.
The kit contained an expired component.
Medline Industries is recalling Centur:ion Silver Antimicrobial VAD Drives with serial number 10653160274841 and lot number 22ABO498 because they contain an expired component. This could pose a risk to medical safety if the device is used improperly.
The kit contains an expired component which could lead to reduced effectiveness of the antimicrobial properties. This might compromise the device's intended medical use, especially in critical care settings.
Healthcare professionals and patients using the Centurion Silver Antimicrobial VAD Drive may be affected. Those with the specific serial number and lot number are most at risk.
Check for the serial number 10653160274841 and lot number 22ABO498 on the Centurion Silver Antimicrobial VAD Drive. The product is sold under the brand Medline Industries.
Look for the serial number 10653160274841 and lot number 22ABO498 on the device.
The recall notice does not specify any action steps.
The product contains an expired component which could reduce its antimicrobial effectiveness, but the recall does not specify serious injury risks.
Check for the serial number 10653160274841 and lot number 22ABO498 on the device.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1015-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1015-2023 from Medline Industries. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
