Medline recalls Centurion OB Instrument Tray (ref MN392:23JBX257, 23KMG455) due to risk of detached trumpet needle guide ring during use.
Trumpet Needle Guide ring can detach when excessive pressure is applied.
Medline is recalling its Centurion OB Instrument Tray (model MN3925) because a trumpet needle guide ring can detach when excessive pressure is applied. This could lead to injury during medical procedures if the ring becomes loose.
The trumpet needle guide ring can detach when excessive pressure is applied during medical procedures. This could cause the ring to become loose, potentially leading to injury if it slips or moves unexpectedly.
Medical professionals using the Centurion OB Instrument Tray for procedures are most at risk. The recall affects specific lot numbers sold in the U.S.
Check for lot numbers 23JBX257 or 23KMG455 on the tray's packaging. The product is a medical procedure convenience tray with UDI/DI numbers 40653160122945 (case) and 10653160122944 (unit).
Inspect the trumpet needle guide ring for signs of detachment or looseness before use.
Reach out to Medline Industries for specific guidance on safe use or replacement options.
The recall states the ring can detach with excessive pressure, so it's not dangerous under normal use but could become a hazard during procedures.
Look for lot numbers 23JBX257 or 23KMG455 on the tray's packaging or UDI/DI numbers 40653160122945 (case) and 10653160122944 (unit).
The recall doesn't specify a remedy, so contact Medline Industries for guidance on safe use or replacement.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1917-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1917-2024 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.
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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.
