Steris recalls certain Hookup Accessories for MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors due to potential label degradation that could delay patient procedures.
Identification label on affected hookups could become illegible over time due to the label's ink coming off. This may potentially prevent users from being able to effectively identify the hookup and may ultimately result in postponement of patient procedures.
Steris is recalling specific Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors. The identification labels on these accessories may become illegible over time because the ink can fade, which could prevent users from identifying the accessories and potentially delay patient procedures.
The identification label on the hookups may fade over time due to the ink coming off. This could make it difficult for users to identify the hookups, which might lead to delays in patient procedures if the correct accessories are not used.
Healthcare facilities that use MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors with the recalled Hookup Accessories are most at risk. These accessories are used in medical procedures involving endoscopes.
Check the model number on the hookups. The affected models are listed in the recall notice, including items like 2-8-001, 2-8-010, 2-8-014, and others. These hookups were distributed between July 17 and September 27, 2023.
Look for the model number on the hookups to determine if they are affected. The affected models are listed in the recall notice.
The identification label on the hookups may become illegible over time because the ink can fade, which could prevent users from identifying the hookups and potentially delay patient procedures.
Check the model number on the hookups. The affected models are listed in the recall notice, including items like 2-8-001, 2-8-010, 2-8-014, and others. These hookups were distributed between July 17 and September 27, 2023.
The recall notice does not specify a remedy, so no action is required beyond checking the model number to confirm if the hookup is affected.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-0617-2024 — Steris Steris Hello, I own a Steris that is covered by recall Z-0617-2024 from Steris. 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.
