Medline recalls Centurion Umbilical Cord Clamp Cutter (CTR300) due to potential weak seal causing sterility breaches. Product code 67335, lot numbers 2023111090. Check if your item has the specified model or lot number.
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Medline is recalling its Centurion Umbilical Cord Clamp Cutter (CTR300) because it may have a weak seal that could breach sterility if the seal fails. This risk is especially concerning for medical use where contamination could lead to infections.
The device may have a weak seal that could fail without being noticeable to the user. If the seal fails, it might allow contamination of the umbilical cord clamp cutter, potentially leading to infections during medical procedures.
Healthcare professionals and medical facilities using the Centurion Umbilical Cord Clamp Cutter (CTR300) with product code 67335 and lot number 2023111090 are most at risk. The recall applies to items sold in the U.S. during the specified production period.
Check for the product code 67335 and lot number 2023111090 on the packaging or label. The device is labeled as Centurion DISP.UMBILICAL CORD CLAMP CUTTER (CTR300).
Look for product code 67335 and lot number 2023111090 on the device or its packaging.
The recall states the device may have a weak seal that could breach sterility if the seal fails, but it does not indicate that the product is unsafe when used correctly.
Check for product code 67335 and lot number 2023111090 on the device or its packaging.
The recall does not specify a remedy, so no action is required beyond checking if your device matches the affected model and lot number.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1451-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1451-2024 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.
