Device does not produce a visual or audible impedance respiration APN alarm when an impedance respiration apnea event occurs.
Device does not produce a visual or audible impedance respiration APN alarm when an impedance respiration apnea event occurs.
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 GE Medical Systems Information Technologies Inc to request your refund or repair — edit it as you like.
Subject: Recall Z-0202-2018 — GE Medical Systems Information Technologies Inc GE Medical Systems Information Technologies, Inc. r Hello, I own a GE Medical Systems Information Technologies, Inc. recalls CARESCAPE Patient Data Module (PDM) v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier that is covered by recall Z-0202-2018 from GE Medical Systems Information Technologies Inc. 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.
