Class I — Flexicare Medical (Dongguan) Ltd.
| Recalling firm | FLEXICARE MEDICAL LTD. |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Laryngoscope handles may not illuminate as intended. |
| Product | BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U |
| Quantity | N/A |
| Distribution | US Nationwide distribution in the states of WA, SD, TX, VA, PA, OK, GA, MI, WY, NC, OH. |
| Initiated | 2025-07-11 |
| Classified | 2025-08-01 |
| Recall number | Z-2184-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — Flexicare Medical (Dongguan) Ltd. (Z-2184-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97139/
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