FDA Device recall Z-0441-2019
Heron toilet and bath chair Model 880505-01 & 880505-11
- FDA Device
- Class II
- ongoing
- Published 2018-11-21
On 2018-11-21 the FDA classified a Class II recall of Heron toilet and bath chair Model 880505-01 & 880505-11 by R82 A S, citing replacement campaign on all units that have a gas spring head in aluminum.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0441-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-06-30 |
| Published | 2018-11-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | R82 A S |
| Distribution | US |
Product
Heron toilet and bath chair Model 880505-01 & 880505-11
Reason
Replacement campaign on all units that have a gas spring head in aluminum.
Identifiers
| code_info | Serial Numbers: 309658, 310007, 319209, 319822, 319823, 319824, 319825, 319826, 319827, 319829, 319830, 319831, 330695,…Serial Numbers: 309658, 310007, 319209, 319822, 319823, 319824, 319825, 319826, 319827, 319829, 319830, 319831, 330695, 330696, 330697, 331862, 331914, 332387, 332586, 332587, 332589, 333755, 333761, 333762, 334833, 342515, 342518, 342523, 345084, 345085 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0441-2019%22
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