Risk of unintended motion while the AIRO system is in transport mode.
Risk of unintended motion while the AIRO system is in transport mode.
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 Brainlab AG to request your refund or repair — edit it as you like.
Subject: Recall Z-0509-2018 — Brainlab AG Brainlab AG recalls AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The A Hello, I own a Brainlab AG recalls AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed that is covered by recall Z-0509-2018 from Brainlab AG. 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.
