Medline recalls sterile ear speculum sets with possible weak seals that could breach sterility. Affected units sold in 2023 with specific lot numbers. Consumers should check product codes 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 sterile ear speculum sets that may have weak seals causing sterility breaches. This could lead to infections if the seal fails during use, especially since the failure might not be noticeable to users.
The speculum set may have a weak seal that could fail, leading to contamination of the contents. This breach might not be detectable by users, increasing infection risk during medical procedures.
Healthcare professionals and patients using the Centur: Sterile Round Ear Speculum Set (3, 4, or 5) with specific lot numbers. Those most at risk are users who rely on the product for medical procedures where sterility is critical.
Check for Product Code I68505 and Lot Numbers 2023090190 or 2023101190. The set includes a case with UDI/DI 00653160294453 and a unit with 10653160294450.
Look for Product Code I68505 and Lot Numbers 2023090190 or 2023101190 on the packaging.
The recall states the product may have a weak seal that could breach sterility, but it is not unsafe for all users. Affected units should be checked for specific lot numbers.
Check for Product Code I68505 and Lot Numbers 2023090190 or 2023101190 on the packaging or case.
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-1433-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1433-2024 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.
