# FDA recall Z-0441-2019

> **R82 A/S** · Class II · device recall initiated 2017-06-30.

## Product

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

## Reason for recall

Replacement campaign on all units that have a gas spring head in aluminum.

## Distribution

Nationwide  Denmark, Germany, Spain, Finland, France, Great Britain, Island, Netherlands, Norway, Poland, Switzerland, Japan, Australia and New Zealand

## Key facts

- **Recall number:** Z-0441-2019
- **Recalling firm:** R82 A/S
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-06-30
- **Report date:** 2018-11-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gedved, Denmark

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0441-2019

## Citation

> AI Analytics. FDA recall Z-0441-2019. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0441-2019. Source: US FDA. Licensed CC0.

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