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 | Terminated |
| Reason | Firm received feedback form the market regarding breakage of the plastic joint which connects the back to the seat. |
| Product | Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 953132-00, 935-135-00, 935136-00, 953211-00, 953221-00, 953222-00, 953225-00, 953226-00, 953231-001, 953232-00, 953236-00 Product Usage: Activity chair (wheelchair) |
| Quantity | 68 units |
| Distribution | US in the states of NC |
| Initiated | 2019-03-28 |
| Classified | 2019-05-11 |
| Terminated | 2023-12-15 |
| Recall number | Z-1315-2019 |
| 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-1315-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82571/
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