FDA Device recall Z-1025-2016
Karma Flexx Wheelchair Manual Wheelchair
- FDA Device
- Class II
- terminated
- Published 2016-03-09
On 2016-03-09 the FDA classified a Class II recall of Karma Flexx Wheelchair Manual Wheelchair by Karman Healthcare, citing karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1025-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-27 |
| Published | 2016-03-09 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Karman Healthcare |
| Distribution | CA, NY, TX, WA |
Product
Karma Flexx Wheelchair Manual Wheelchair.
Reason
Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.
Identifiers
| code_info | Item # 935-0245H6 Flexx (KM852216) Serial # TM14-A03982-TM14-A03991 Item # 935-0246H6 Flexx (KM852218) Serial…Item # 935-0245H6 Flexx (KM852216) Serial # TM14-A03982-TM14-A03991 Item # 935-0246H6 Flexx (KM852218) Serial # TM14-A03992-TM14-A04012 Item # 935-0247H6 Flexx (KM852220) Serial # TM14-A4013-TM14-A04017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1025-2016%22
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