Facility
Drive DeVilbiss Healthcare
3 recall(s) on record — most severe on record: Class I.
| FDA Establishment Identifier (FEI) | 3015772781 |
|---|---|
| Establishment type | Repack or Relabel Medical Device |
| Location | 500 Palmetto Logistics Parkway Palmetto, GA, US 30268 |
| Registration status | Active · expires 2026 |
| Parent company | Medical Depot Inc dba Drive DeVilbiss Healthcare (owner-operator 9040780) |
Devices registered here (2)
- Nebulizer (Direct Patient Interface)Product code CAF · Class II · Anesthesiology · 21 CFR 868.5630
- Compressor, Air, PortableProduct code BTI · Class II · Anesthesiology · 21 CFR 868.6250
Recalls & enforcement
- Class IOngoing2025-04-11Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
- Class IIOngoing2024-06-14The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
- Class IITerminated2016-02-17Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Related
- All facilities operated by Medical Depot Inc dba Drive DeVilbiss Healthcare
- Drive Northpoint, LLC (GA)
- Drive DeVilbiss Healthcare (NJ)
- Drive DeVilbiss Healthcare (CA)
- STME Acquisition LLC (GA)
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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