Data Foundry

Medical device recalls 2024

Brand Name: NOVA ORTHO-MED INC — Class II medical device recall Z-0131-2025

Ongoing recall by Nova Ortho-Med Inc, reported 2024-10-23, distributed nationwide. Firm identified a potential risk for a fall hazard. When the end user is readjusting from the slouched seated

Recall numberZ-0131-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmNova Ortho-Med Inc, Carson, CA, United States
Recall initiated2024-08-26
Classified2024-10-17
Reported by FDA2024-10-23
DistributedNationwide (US)
Countries outside the USCA
Quantity1,585
UPC / GTIN / UDI-DI00652308012263
Model numbers4329RD

Product

Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR RED Model/Catalog Number: 4329RD 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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0131-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.