A software anomaly in the 731 software version 05/20/00, was identified, which can lead to a user inadvertently changing device settings.
A software anomaly in the 731 software version 05/20/00, was identified, which can lead to a user inadvertently changing device settings.
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 ZOLL Medical Corporation to request your refund or repair — edit it as you like.
Subject: Recall Z-0812-2018 — ZOLL Medical Corporation ZOLL Medical Corporation recalls 731 Series Ventilators running software v Hello, I own a ZOLL Medical Corporation recalls 731 Series Ventilators running software version 05.20.00 The devices in the ZOLL ventilator are indicated for use in that is covered by recall Z-0812-2018 from ZOLL Medical 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.
