Invacare Corporation: Invacare Storm TDX Power Wheelchair, Models: #TDX3-PS, TDX3-SE-PS, TDX4-PS.

Recall number

Z-0966-2007

Recalling firm

Invacare Corporation

Product

Invacare Storm TDX Power Wheelchair, Models: #TDX3-PS, TDX3-SE-PS, TDX4-PS.

Status

Terminated

Initiated

2007-03-19

Posted

2007-07-04

Terminated

2012-09-27

Reason

Software error may permit the chair to recline too far.

Root cause

Other

Action

The recalling firm sent a recall letter dated March 19, 2007. The recalling firm also posted information regarding the recall on their website.

Quantity

227 devices

Distribution

Nationwide and Canada.

Lot, serial or model codes

06JE002273, 06JE002762, 06JE003580, 06JE003583, 06JE003584, 06JE003585, 06JE003597, 06JE003598, 06JE003880, 06JE003890, 06JE004170, 06JE004172, 06JE004178, 06JE004196, 06JE004632, 06JE004640, 06JE005420, 06JE005421, 06JE005864, 06JE005870, 06JE005871, 06JE005879, 06JE005885, 06JE006254, 06JE006277, 06JE006599, 06JE006603, 06JE006612, 06JE007087, 06JE007393, 06JE007396, 06JE007403, 06JE007408, 06JE007818, 06JE008028, 06JE008311, 06JE008322, 06JE008324, 06JE008329, 06JE008330, 06JE008332, 06JE008350, 06JE008670, 06JE008678, 06JE009028, 06JE009031, 06JE009039, 06JE009040, 06JE009042, 06JE009060, 06JE009062, 06JE009076,  06KE000147, 06KE000149, 06KE001924, 06KE001933, 06KE002243, 06KE002264, 06KE002265, 06KE002267, 06KE002270, 06KE002851, 06KE002853, 06KE002858, 06KE002862, 06KE003116, 06KE003379, 06KE003381, 06KE003386, 06KE003612, 06KE004451, 06KE004454, 06KE004455, 06KE004467, 06KE004854, 06KE005538, 06KE005826, 06KE006063, 06KE006065, 06KE006333, 06KE006613, 06KE006876, 06KE006877, 06KE006886, 06KE006894, 06KE007257, 06KE007282, 06KE007294, 06KE007450, 06KE007684, 06KE007686, 06KE007689, 06KE008610, 06KE008611, 06LE000170, 06LE000173 06LE001305, 06LE001313, 06LE001527, 06LE001694, 06LE001696, 06LE001697, 06LE001705, 06LE001998, 06LE002608, 06LE003258, 06LE003261, 06LE003267, 06LE003268, 06LE003462, 06LE003466, 06LE003987, 06LE004643, 06LE004650, 06LE004846, 06LE004857, 06LE005143, 06LE005144, 06LE005148, 06LE005152, 06LE005154, 06LE005732, 06LE005895, 06LE006012, 06LE006013, 06LE006024, 06LE006704, 06LE006707, 06LE006709, 06LE007018, 06LE007210, 06LE007358, 06LE007371, 06LE007379, 06LE007387, 06LE007393, 06LE007397, 06LE007403, 06LE007404, 07AE000983, 07AE001149, 07AE001180, 07AE001326, 07AE001327, 07AE001334, 07AE001594, 07AE001595, 07AE002009, 07AE002013, 07AE002223, 07AE002225, 07AE002229, 07AE002400, 07AE002404, 07AE002670, 07AE002683, 07AE002990, 07AE003522, 07AE003700, 07AE003712, 07AE003713, 07AE003716, 07AE004618, 07AE005103, 07AE005337, 07AE005339, 07AE005340, 07AE005341, 07AE005586, 07AE005593, 07AE005597, 07AE005886, 07AE005887, 07AE005895, 07AE006089, 07AE006303, 07AE006308, 07AE006314, 07AE006927, 07AE006930, 07AE007089, 07AE007090, 07AE007091, 07AE007092, 07AE007103, 07AE007105, 07AE007113, 07AE007114, 07AE007326, 07AE007327, 07AE007331, 07AE007334, 07AE007598, 07AE007606, 07AE007607, 07AE007611, 07AE007612, 07BE001073, 07BE001076, 07BE001077, 07BE001078, 07BE001082, 07BE001093, 07BE001303, 07BE001309, 07BE001310, 07BE001578, 07BE001585, 07BE001806, 07BE001810, 07BE002005, 07BE002014, 07BE002015, 07BE002253, 07BE002254, 07BE003336, 07BE003337, 07BE003569, 07BE003574, 07BE003582, 07BE003584, 7BE003585, 07BE004719, 07BE004907, 07BE004913, 07BE004916, 07BE006332.

510(k) numbers

["K023589"]

PMA numbers

not on file

Product code

ITI

Firm FEI

3002889431

Firm city

Elyria

Firm state

OH

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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