Flexicare Medical (Dongguan) Ltd.: Device Recall

Recall #Z-2186-2025 · 07/11/2025

Class I: Dangerous

Recall Details

Recall Number: Z-2186-2025
Classification: Class I
Product Type: Device
Recalling Firm: Flexicare Medical (Dongguan) Ltd.
Status: Ongoing
Date Initiated: 07/11/2025
Location: Dongguan, N/A, China
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: N/A

Reason for Recall

Laryngoscope handles may not illuminate as intended.

Product Description

BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U

Distribution Pattern

US Nationwide distribution in the states of WA, SD, TX, VA, PA, OK, GA, MI, WY, NC, OH.

Other Recalls by Flexicare Medical (Dongguan) Ltd.

Class I: Dangerous 07/11/2025

Laryngoscope handles may not illuminate as intended.
Class I: Dangerous 07/11/2025

Laryngoscope handles may not illuminate as intended.
Class I: Dangerous 07/11/2025

Laryngoscope handles may not illuminate as intended.
Class I: Dangerous 07/11/2025

Laryngoscope handles may not illuminate as intended.
Class I: Dangerous 07/11/2025

Laryngoscope handles may not illuminate as intended.

View all recalls by Flexicare Medical (Dongguan) Ltd. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.