FDA Device recall Z-2294-2019

TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-…

FDA Device
Class II
terminated
Published 2019-08-28

On 2019-08-28 the FDA classified a Class II recall of TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-… by Tisport, citing the anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2294-2019
Classification	Class II
Status	terminated
Initiated	2018-09-11
Published	2019-08-28
Last updated	2026-09-13 11:55 UTC
Company	Tisport
Distribution	US

Product

TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs). Product Usage: The affected component is part of a manual wheelchair to provide mobility to physically impaired individuals. The affected component is used to prevent the wheelchair from tipping backwards.

Reason

The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.

Identifiers

code_info	11908818, 11914822, 11918140, 11922587, 11927950, 11928694, 11931072, 11931597, 11935222, 11936116, 11937341, 11944462,… 11908818, 11914822, 11918140, 11922587, 11927950, 11928694, 11931072, 11931597, 11935222, 11936116, 11937341, 11944462, 11946693, 11946914, 11948640, 11958774, 11961303, 11963610, 11971197, 11972416, 11973295, 11973373, 11982499, 11988601, 11992794, 11994940, 11995536, 11995570, 11996713, 11996864, 12005061, M2005478, M2005586, M2019937, M2019958, M2019959, M2019961, M2019968, M2019996, M2021020, M2021023, M2021026, M2021029, M2021030, M2021038, M2021044, M2021048, M2021049, M2021063, M2021069, M2021077, M2021078, M2021097, M2021105, M2021115, M2021117, M2021120, M2021124, M2021130, M2021144, M2021146, M2021150, M2021155, M2021166, M2021170, M2021173, M2021180, M2021181, M2021186, M2021187, M2021194, M2021215, M2021219, M2021229, M2021230, M2021231, M2021233, M2021237, M2021244, M2021246, M2021259, M2021271, M2021272, M2021280, M2021281, M2021286, M2021287, M2021300, M2021301, M2021302, M2021304, M2021307, M2021328, M2021348, M2021351, M2021362, M2021366, M2021367, M2021370, M2021371,

code_info

11908818, 11914822, 11918140, 11922587, 11927950, 11928694, 11931072, 11931597, 11935222, 11936116, 11937341, 11944462,…

11908818, 11914822, 11918140, 11922587, 11927950, 11928694, 11931072, 11931597, 11935222, 11936116, 11937341, 11944462, 11946693, 11946914, 11948640, 11958774, 11961303, 11963610, 11971197, 11972416, 11973295, 11973373, 11982499, 11988601, 11992794, 11994940, 11995536, 11995570, 11996713, 11996864, 12005061, M2005478, M2005586, M2019937, M2019958, M2019959, M2019961, M2019968, M2019996, M2021020, M2021023, M2021026, M2021029, M2021030, M2021038, M2021044, M2021048, M2021049, M2021063, M2021069, M2021077, M2021078, M2021097, M2021105, M2021115, M2021117, M2021120, M2021124, M2021130, M2021144, M2021146, M2021150, M2021155, M2021166, M2021170, M2021173, M2021180, M2021181, M2021186, M2021187, M2021194, M2021215, M2021219, M2021229, M2021230, M2021231, M2021233, M2021237, M2021244, M2021246, M2021259, M2021271, M2021272, M2021280, M2021281, M2021286, M2021287, M2021300, M2021301, M2021302, M2021304, M2021307, M2021328, M2021348, M2021351, M2021362, M2021366, M2021367, M2021370, M2021371,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2294-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.