BOMImed Disposable Fiber Optic Medium Laryngoscope Handle — Class II medical device recall Z-3238-2017
Terminated recall by Bomimed, reported 2017-10-11, distributed in IL, PA, WA. Potential for intermittent lighting (flickering) during use.
| Recall number | Z-3238-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bomimed, Winnipeg, N/A, Canada |
| Recall initiated | 2017-07-13 |
| Classified | 2017-09-29 |
| Reported by FDA | 2017-10-11 |
| Terminated | 2021-04-01 |
| Distributed | IL, PA, WA |
| Countries outside the US | CA |
| Lot numbers | 2216, 3016, 4016, 4816 |
| Model numbers | OL-334L6 |
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.
Reason for recall
Potential for intermittent lighting (flickering) during use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3238-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.