Facility
PDG PRODUCT DESIGN GROUP, INC.
2 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 3003748905 |
|---|---|
| Establishment type | Manufacture Medical Device |
| Location | 14273 Knox Way Richmond British Columbia, CA V6V 2Z4 |
| Registration status | Active · expires 2026 |
| Parent company | Permobil Inc (owner-operator 9025865) |
| Brand names | Eclipse 350 |
Devices registered here (1)
- Wheelchair, MechanicalProduct code IOR · Class I · Physical Medicine · 21 CFR 890.3850
Recalls & enforcement
- Class IITerminated2018-08-15This correction decision has been made because of a potential failure of one or both backrest bars providing back support. If one or both back support telescoping bars fail the user could fall back leading to a potential injury.
- Class IITerminated2017-09-01There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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