Class II — Karman Healthcare Inc
| Recalling firm | KARMAN HEALTHCARE, INC. |
|---|---|
| Registered facility | KARMAN HEALTHCARE INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets. |
| Product | Karma Flexx Wheelchair Manual Wheelchair. |
| Quantity | 35 |
| Distribution | U.S. distribution to the following states -- WA, CA, NY, and TX. |
| Initiated | 2016-01-27 |
| Classified | 2016-02-27 |
| Terminated | 2016-06-29 |
| Recall number | Z-1025-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Karman Healthcare Inc (Z-1025-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73159/
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