Fuze Manual Tilt Wheelchair — Class II medical device recall Z-2695-2014
Terminated recall by Pdg Product Design Group Inc, reported 2014-10-01, distributed in AZ, CA, GA, KY, MI, MN, MO, MS…. The hex bolt head might shear and cause the axle plate to detach from the lower frame of the wheelchair and co
| Recall number | Z-2695-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pdg Product Design Group Inc, Vancouver, British Columbia, Canada |
| Recall initiated | 2012-06-12 |
| Classified | 2014-09-24 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2015-07-23 |
| Distributed | AZ, CA, GA, KY, MI, MN, MO, MS, NC, NE, NY, OH, PA, SC, TX, VA, WA |
| Countries outside the US | CA, HK |
| Quantity | 153 |
| Reason classes | device malfunction |
Product
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Reason for recall
The hex bolt head might shear and cause the axle plate to detach from the lower frame of the wheelchair and could collapse the wheels while in use.
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-2695-2014. 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.