RecallRadar

FDA Device recall Z-0441-2019

Heron toilet and bath chair Model 880505-01 & 880505-11

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

AgencyFDA Device
Recall numberZ-0441-2019
ClassificationClass II
Statusongoing
Initiated2017-06-30
Published2018-11-21
Last updated2026-09-13 11:54 UTC
CompanyR82 A S
DistributionUS

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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.