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

Recall Z-2187-2025 — BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U

U.S. FDA — Device Enforcement · China · 2025-07-11 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2187-2025
Date of alert
2025-07-11
Country / jurisdiction
China
Risk level
Class I
Risk type
recall
Brand
Flexicare Medical (Dongguan) Ltd.
Product category
device
Product type
Devices
Reported risk: Laryngoscope handles may not illuminate as intended.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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