Class I

Medical Device Recall: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle REF:040-03-0000U

Flexicare Medical (Dongguan) Ltd. · July 11, 2025

Reason for Recall

Laryngoscope handles may not illuminate as intended.

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

N/A

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2185-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Flexicare Medical (Dongguan) Ltd. Medical Device Recall: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle REF:040-03-0000U | SafeCheck