Flexicare Medical (Dongguan) recalls
Flexicare Medical (Dongguan) has 6 recalls on record with the FDA and USDA, the earliest in 2025 and the latest reported on 13 Aug 2025. 6 are still ongoing. The most frequent reason is device malfunction.
Total recalls6since 2025
Last 12 months0reported
Class I6100% of total
Ongoing6latest 13 Aug 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 6 100%Class II 0 0%Class III 0 0%
Why flexicare medical (dongguan) is recalled
Product types
By year
Ongoing flexicare medical (dongguan) recalls
6 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Single-Use Fiber Optic Handle and Blade Refs recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Single-Use Fiber Optic Laryngoscope Handle recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Mini with Pro Miller Blade Size recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Single-Use Fiber Optic Mini Handle and Blade recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
All flexicare medical (dongguan) recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Single-Use Fiber Optic Handle and Blade Refs recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Single-Use Fiber Optic Laryngoscope Handle recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Mini with Pro Miller Blade Size recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
| Device | CLASS I | BritePro Solo Single-Use Fiber Optic Mini Handle and Blade recalled | Flexicare Medical (Dongguan) | Device Malfunction | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.