FDA Device recall Z-3238-2017
BOMImed Disposable Fiber Optic Medium Laryngoscope Handle
- FDA Device
- Class II
- terminated
- Published 2017-10-11
On 2017-10-11 the FDA classified a Class II recall of BOMImed Disposable Fiber Optic Medium Laryngoscope Handle by Bomimed, citing potential for intermittent lighting (flickering) during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3238-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-13 |
| Published | 2017-10-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Bomimed |
| Distribution | IL, PA, WA |
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
Potential for intermittent lighting (flickering) during use.
Identifiers
| code_info | Part number: OL-334L6 Lot#: 2216, 3016, 4016 and 4816 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3238-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.