Facility
GETINGE AB
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 3031563141 |
|---|---|
| Establishment type | Complaint File Establishment per 21 CFR 820.198 |
| Location | KOPANINA 30A POZNAN Wielkopolskie, PL 60105 |
| Registration status | Active · expires 2026 |
| Parent company | Getinge AB (owner-operator 10090886) |
| Brand names | Rigid Head Rest 1002.82A0; 1180 52A0 Multimodality Headrest, Fixed |
Devices registered here (1)
- Holder, Head, RadiographicProduct code IWY · Class I · Radiology · 21 CFR 892.1920
Recalls & enforcement
- Class IITerminated2021-04-15There is a potential for abnormal inflation of the mattress.
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-15. Verify this facility record at FDA →
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