Class II — Bomimed
| Recalling firm | BOMIMED INC. |
|---|---|
| Registered facility | BOMIMED INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for intermittent lighting (flickering) during use. |
| Product | BOMImed Disposable Fiber Optic Medium Laryngoscope Handle. Each handle is packaged in an individual peel pouch, 20 handles per box. The rigid laryngoscope handle is a device used along with a blade to examine and visualize a patient's airway and aid placement of a tracheal tube. |
| Quantity | 680 (US) 2,220 (OUS) |
| Distribution | IL. PA. and WA CANADA |
| Initiated | 2017-07-13 |
| Classified | 2017-09-29 |
| Terminated | 2021-04-01 |
| Recall number | Z-3238-2017 |
| 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 II recall — Bomimed (Z-3238-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77958/
Alerts for BOMIMED INC.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.