Medline recalls Centurion Curette kits with weak seals that could breach sterility. Affected kits have specific product codes and lot numbers. Consumers should check their kits and contact Medline for details.
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 certain Centurion Curette kits due to a weak seal that might cause the contents to become non-sterile if the seal fails. This could lead to infection or other health risks during dental procedures. The recall affects specific product models and lot numbers.
The kits may have a weak seal that could breach sterility if the seal fails. This failure might not be detectable by all users, potentially leading to non-sterile contents during dental procedures.
Dental professionals and patients using the recalled Centurion Curette kits. Those with the specific product codes and lot numbers listed in the recall are most at risk.
Check for product codes 66745, 67050, 67430, I67970, I68040, I68340, I68380, I68470, or I68480 with specific lot numbers listed in the recall notice.
Look for the product code and lot numbers on the kit packaging to confirm if it is affected.
The recall states the kits may have a weak seal that could breach sterility, so they are not safe to use without checking the recall list.
Check the product code and lot numbers listed in the recall notice to see if your kit matches the affected models.
The recall does not specify a remedy, so contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1439-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1439-2024 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.
