Skip to the content

FDA Medical Device Recalls (openFDA)

Invacare Corporation: Kuschall K Junior Manual wheelchair

Recall number
Z-0421-2010
Recalling firm
Invacare Corporation
Product
Kuschall K Junior Manual wheelchair
Status
Terminated
Initiated
2009-06-15
Posted
2009-11-25
Terminated
2011-11-21
Reason
The handle has been breaking at a calculated weight of 65 kg which may have serious consequences (broken bones) depending on the circumstances of the break (e.g., user on ramps, hills, etc.).
Root cause
Device Design
Action
The firm contacted their customers by telephone and then sent a recall notification letter to each customer on 6/15/2009. Questions are directed to email: Recalls@Invacare.com or phone: 800-333-6900.
Quantity
20 Wheelchairs
Distribution
Product was distributed to the following states: CA, CO, MN, NJ, OR, PA, TX & VA and one to Canada.
Lot, serial or model codes
Model Numbers: 0806281234, 0806893858, 0806135534, 0806161578, 0806237627, 0806268153, 0806268154, 0806309590, 0806315524, 0806351557, 0806568768, 0806591793. 0806670117, 0806724855, 0806731287, 0806773921, 0807007811, 0807019897, 0807062866, 0807110193
510(k) numbers
["K982336"]
PMA numbers
not on file
Product code
IOR
Firm FEI
3002889431
Firm city
Elyria
Firm state
OH
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

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

Search this register