Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.
Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Steris Corporation to request your refund or repair — edit it as you like.
Subject: Recall Z-0772-2018 — Steris Corporation Steris Corporation recalls V-PRO 60 Low Temperature Sterilization System (UDI: 0 Hello, I own a Steris Corporation recalls V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) that is covered by recall Z-0772-2018 from Steris Corporation. 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.
