Invacare recalls AVIVA Storm RX wheelchairs with LiNX Gyro firmware 6.1.2 due to potential injury from aggressive deceleration. Affected models include SRX-20R, SRX-20SP, SRX-20MP.
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury
Invacare is recalling AVIVA Storm RX wheelchairs with LiNX Gyro firmware version 6.1.2 because they may decelerate too quickly, causing injury. This affects specific models sold with certain UDI-DI numbers.
The wheelchair's LiNX Gyro system may decelerate more aggressively than intended due to a firmware error. This could cause the user to lose balance or fall, leading to injury.
People using Invacare AVIVA Storm RX wheelchairs with LiNX Gyro Module models DLX-GRY100-A or DLX-GRY101-A are affected. Users with the specific model numbers SRX-20R, SRX-20SP, or SRX-20MP are most at risk.
Check if your wheelchair has model numbers SRX-20R, SRX-20SP, or SRX-20MP. Look for LiNX Gyro Module model numbers DLX-GRY100-A or DLX-GRY101-A. The UDI-DI numbers listed in the recall include specific combinations.
Look for the LiNX Gyro firmware version on your wheelchair's settings menu or documentation.
Reach out to Invacare directly for assistance with firmware updates or replacements.
Yes, the recall states that the wheelchair may decelerate too quickly, potentially causing injury.
The affected models are SRX-20R, SRX-20SP, and SRX-20MP with LiNX Gyro Module models DLX-GRY100-A or DLX-GRY101-A.
The recall does not specify firmware update instructions; contact Invacare directly for assistance.
We’ve drafted a message you can send Invacare to request your refund or repair — edit it as you like.
Subject: Recall Z-0447-2022 — Invacare Invacare Hello, I own a Invacare that is covered by recall Z-0447-2022 from Invacare. 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.
