Invacare Corporation: Medical Device Recall in 2022 - (Recall #: Z-0446-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C

Product Classification:

Class II

Date Initiated: November 12, 2021

Date Posted: January 12, 2022

Recall Number: Z-0446-2022

Event ID: 89062

Reason for Recall:

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

Status: Ongoing

Product Quantity: 303 units US; 20 units OUS

Code Information:

LiNX Gyro firmware version 6.1.2 UDI-DI Numbers: IFX-20C 00841447111627 IFX-20MP 00841447111658 IFX-20R 00841447111634 IFX-20SP 00841447111641 IFX20WIDE 00841447111658

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Canada, Australia, Thailand, New Zealand.

Voluntary or Mandated:

Voluntary: Firm initiated