GlideScope AVL Video Laryngoscope — Class II medical device recall Z-0421-2016
Terminated recall by Verathon, Inc., reported 2015-12-23, distributed nationwide. Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blades may separate, due to inadequat
| Recall number | Z-0421-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Verathon, Inc., Bothell, WA, United States |
| Recall initiated | 2015-11-30 |
| Classified | 2015-12-15 |
| Reported by FDA | 2015-12-23 |
| Terminated | 2016-08-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, BE, BG, BH, BM, CA, CN, CZ, DE, DK, ES, FR, GR, ID, IL, IN, IR, IT, JP, KR, KW, LB, MA, MY, PA, PE, PH, RS, SA, SG, TH, TR, TW, ZA |
| Model numbers | 0574-0115 |
Product
GlideScope AVL Video Laryngoscope (AVL), Part Number AVL 3- 0574-0115; AVL 4-0574-0116, AVL 5- 0574-0117. AVL is a video laryngoscope that incorporates a high resolution color camera, an LED light source and video output to a remote monitor. This system has a digital platform.
Reason for recall
Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blades may separate, due to inadequate bonding of the silicone adhesive affixing the halves of the blade. The potential for blade separation may not be readily visible during routine inspection before or after intubation.
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-0421-2016. 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.