Home › MACHIDA ENDOSCOPE CO.,LTD. › MACHIDA
MACHIDA
MACHIDA ENDOSCOPE CO.,LTD. · Model VSP-2000 · UDI-DI 04580137733041
1
510(k) clearances
157
Adverse events (13 deaths)
2
Recalls
14
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-12-06 | Karl Storz Endoscopy | The firm has become aware that there is a potential that the glass cover at the distal end of the camera/led lighting on the video laryngoscope could become loose during reprocessi |
| 2010-12-08 | Bomimed Inc | On 9/1/2010 BOMImed, Inc. Winnipeg, MB, Canada initiated a recall of their BOMImed Integrated Reusable Laryngoscope Blades (Macintosh & Miller styles - all sizes), Model #OL-32D0 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.