Steris recalls AMSCO 7053HP Washer/Disinfector units due to potential electrical arcing inside the device. This could cause internal damage but poses no risk of electric shock to users.
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
Steris is recalling AMSCO 7053HP Washer/Disinfector units because a wire may shift, causing internal electrical arcing. This hazard is contained within the unit and does not pose a risk of electric shock to users.
The wire connected to the electrical box may shift out of position, causing electrical arcing inside the unit. This arcing is contained within the device and does not pose a risk of electric shock to users.
Healthcare facilities using the AMSCO 7053HP Washer/Disinfector for surgical instrument cleaning are most at risk. The recall affects specific units with serial numbers listed in the official notice.
Check for the model number 7053HP on the unit. Affected units have specific serial numbers listed in the recall notice, including 3619725008, 3619725011, and others.
Look for the serial numbers listed in the recall notice: 3619725008, 3619725011, 3619725013, and others.
No, the electrical arcing remains internal within the unit and does not pose a risk of electric shock to users.
Check the unit's serial number against the list provided in the recall notice to determine if it is affected.
The affected units have specific serial numbers listed in the recall notice, including 3619725008, 3619725011, and others.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-0910-2026 — Steris Steris Hello, I own a Steris that is covered by recall Z-0910-2026 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.
