Steris recalls AMSCO 5000 Series Washer/Disinfector Model #5052 due to software issues that may cause medical instruments to be inadequately cleaned or disinfected. Affected units have specific serial numbers listed in the recall.
The software in the systems may not process the cycle originally intended. This could result in damage to the various medical devices and instruments processed in the washer/disinfector or potential for inadequate cleaning or disinfection.
Steris is recalling AMSCO 5000 Series Washer/Disinfector Model #5052 because software problems might lead to medical instruments not being cleaned or disinfected properly. This could pose a risk to patient safety if instruments are used without adequate sterilization.
The software may not process the intended cleaning cycles correctly, which could result in medical instruments being inadequately cleaned or disinfected. This means instruments might not be safe for reuse, potentially leading to infections or cross-contamination.
Healthcare facilities using the AMSCO 5000 Series Washer/Disinfector Model #5052 are most at risk, particularly those processing medical instruments where proper disinfection is critical.
Check for the model number 'AMSCO 5000 Series' and serial numbers listed in the recall (e.g., 3627418005, 3601518006, etc.). The product was sold by Steris Corporation.
Verify your unit's serial number against the list provided in the recall to confirm if it is affected.
Reach out to Steris Corporation directly for specific instructions on how to address the software issue.
The recalled product is the AMSCO 5000 Series Washer/Disinfector Model #5052.
Check your serial number against the list of affected serial numbers provided in the recall (e.g., 3627418005, 3601518006, etc.).
Contact Steris Corporation directly for specific instructions on addressing the software issue.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-0996-2019 — Steris Steris Hello, I own a Steris that is covered by recall Z-0996-2019 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.
