Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0654-2021 — Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)

U.S. FDA — Device Enforcement · United States · 2019-10-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0654-2021
Date of alert
2019-10-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Nova Ortho-Med Inc
Product category
device
Product type
Devices
Reported risk: Walkers within the identified serial range have the potential for the front fork to unscrew itself from the leg. A partially unscrewed fork creates unevenness in the wheelbase, which could cause instability, that if not detected by the user, may result in the front fork falling off the walker.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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