# FDA recall Z-2445-2023

> **Invacare Corporation** · Class II · device recall initiated 2023-06-15.

## Product

DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat.   Model Number(s):  1654807 - DOLOMITE GLOSS 680 ROLLATOR  1655081 - DOLOMITE GLOSS 600 ROLLATOR  1655082 - DOLOMITE GLOSS 520 ROLLATOR  1655083 - DOLOMITE GLOSS 450 ROLLATOR

## Reason for recall

Premature failure of the seat during use, the plastic eyelets of the folding mechanism of the device's seat can break, and in a worst-case crossbar also breaks and the Rollator can collapse causing injury to user

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2445-2023
- **Recalling firm:** Invacare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-15
- **Report date:** 2023-08-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Elyria, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2445-2023

## Citation

> AI Analytics. FDA recall Z-2445-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2445-2023. Source: US FDA. Licensed CC0.

---

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