Karma Flexx Wheelchair Manual Wheelchair — Class II medical device recall Z-1025-2016
Terminated recall by Karman Healthcare Inc, reported 2016-03-09, distributed in CA, NY, TX, WA. Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding ha
| Recall number | Z-1025-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Karman Healthcare Inc, City of Industry, CA, United States |
| Recall initiated | 2016-01-27 |
| Classified | 2016-02-27 |
| Reported by FDA | 2016-03-09 |
| Terminated | 2016-06-29 |
| Distributed | CA, NY, TX, WA |
| Quantity | 35 |
| Serial numbers | TM14-A03982-TM14-A03991, TM14-A03992-TM14-A04012, TM14-A4013-TM14-A04017 |
| Model numbers | 935-0245H6, 935-0246H6, 935-0247H6 |
Product
Karma Flexx Wheelchair Manual Wheelchair.
Reason for recall
Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1025-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.