Class II — R82 A/S
| Recalling firm | R82 A/S |
|---|---|
| Registered facility | R82 A/S (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Replacement campaign on all units that have a gas spring head in aluminum. |
| Product | Heron toilet and bath chair Model 880505-01 & 880505-11 |
| Quantity | 687 |
| Distribution | Nationwide Denmark, Germany, Spain, Finland, France, Great Britain, Island, Netherlands, Norway, Poland, Switzerland, Japan, Australia and New Zealand |
| Initiated | 2017-06-30 |
| Classified | 2018-11-09 |
| Recall number | Z-0441-2019 |
| 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 — R82 A/S (Z-0441-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81217/
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