A software issue may result in the previous settings being applied instead of the default settings or the unit may skip the startup leak test.
A software issue may result in the previous settings being applied instead of the default settings or the unit may skip the startup leak test.
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 Mindray DS USA, Inc. dba Mindray North America to request your refund or repair — edit it as you like.
Subject: Recall Z-0846-2018 — Mindray DS USA, Inc. dba Mindray North America Mindray DS USA, Inc. dba Mindray North America recal Hello, I own a Mindray DS USA, Inc. dba Mindray North America recalls A-Series A3/A5 Anesthesia Delivery System; Model Numbers: 0633F-01000-0X (A3) and 0631F-01000-0X (A5) Product Usage: that is covered by recall Z-0846-2018 from Mindray DS USA, Inc. dba Mindray North America. 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.
