BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref: 040-02-0110U (Mac 1), 040-02-0120U (Mac 2), 040-02-0130U (Mac 3), 040-02-0131U (Mac 3 Strong Curve) 040-02-0140U (Mac 4), 040-02-0400U (Miller 00), 040-02-0410U (Miller 1), 040-02-0420U (Miller 2), 040-02-0430U (Miller 3),
Reported: August 13, 2025 Initiated: July 11, 2025 #Z-2182-2025
Product Description
BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref: 040-02-0110U (Mac 1), 040-02-0120U (Mac 2), 040-02-0130U (Mac 3), 040-02-0131U (Mac 3 Strong Curve) 040-02-0140U (Mac 4), 040-02-0400U (Miller 00), 040-02-0410U (Miller 1), 040-02-0420U (Miller 2), 040-02-0430U (Miller 3),
Reason for Recall
Laryngoscope handles may not illuminate as intended.
Details
- Recalling Firm
- Flexicare Medical (Dongguan) Ltd.
- Units Affected
- N/A
- Distribution
- US Nationwide distribution in the states of WA, SD, TX, VA, PA, OK, GA, MI, WY, NC, OH.
- Location
- Dongguan, N/A
Frequently Asked Questions
What product was recalled? ▼
BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref: 040-02-0110U (Mac 1), 040-02-0120U (Mac 2), 040-02-0130U (Mac 3), 040-02-0131U (Mac 3 Strong Curve) 040-02-0140U (Mac 4), 040-02-0400U (Miller 00), 040-02-0410U (Miller 1), 040-02-0420U (Miller 2), 040-02-0430U (Miller 3),. Recalled by Flexicare Medical (Dongguan) Ltd.. Units affected: N/A.
Why was this product recalled? ▼
Laryngoscope handles may not illuminate as intended.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 13, 2025. Severity: Critical. Recall number: Z-2182-2025.
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