# FDA recall Z-0129-2025

> **Nova Ortho-Med Inc** · Class II · device recall initiated 2024-08-26.

## Product

Brand Name: NOVA ORTHO-MED INC.  Product Name: MONARCH ROLLATOR BLUE  Model/Catalog Number: 4329BL  Product Description: ROLLING WALKER MOBILITY AID

## Reason for recall

Firm identified a potential risk for a fall hazard. When the end user is readjusting from the slouched seated position to an upright seated position, there is the potential for the movement to cause the backrest to lift out of the backrest holder and disengage from the unit.

## Distribution

Worldwide - U.S. Nationwide distribution including in the states of AK, AL AZ, CA, CO, CT, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SD, TN, TX, UT, VA, WA, WI and WY. The country of Canada.

## Key facts

- **Recall number:** Z-0129-2025
- **Recalling firm:** Nova Ortho-Med Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-26
- **Report date:** 2024-10-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Carson, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0129-2025

## Citation

> AI Analytics. FDA recall Z-0129-2025. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0129-2025. Source: US FDA. Licensed CC0.

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