# FDA recall Z-1315-2019

> **R82 A/S** · Class II · device recall initiated 2019-03-28.

## 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)

## Reason for recall

Firm received feedback form the market regarding breakage of the plastic joint which connects the back to the seat.

## Distribution

US in the states of NC

## Key facts

- **Recall number:** Z-1315-2019
- **Recalling firm:** R82 A/S
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-28
- **Report date:** 2019-05-22
- **Termination date:** 2023-12-15

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1315-2019

## Citation

> AI Analytics. FDA recall Z-1315-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1315-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*