BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U
Class I - Dangerous 🏥 Medical Devices
Recalled: July 11, 2025 Flexicare Medical (Dongguan) Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: Lots: 2007xxxxx to 2012xxxxx (July-2020 to Dec-2020)
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Flexicare Medical (Dongguan) Ltd.
- Reason for Recall:
- Laryngoscope handles may not illuminate as intended.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U
Product Codes/Lot Numbers:
Lots: 2007xxxxx to 2012xxxxx (July-2020 to Dec-2020)
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2186-2025
Related Recalls
Class I - Dangerous
Laryngoscope handles may not illuminate as intended.
BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U
Flexicare Medical (Dongguan)
Class I - Dangerous
Laryngoscope handles may not illuminate as intended.
BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U
Flexicare Medical (Dongguan)
Class I - Dangerous
Laryngoscope handles may not illuminate as intended.