It is recommended for patients with weight/size between 4-22 lbs — Class II medical device recall Z-1852-2017
Terminated recall by Verathon Inc, reported 2017-04-26, distributed nationwide. Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged with the incorrect size device (G
| Recall number | Z-1852-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Verathon Inc, Bothell, WA, United States |
| Recall initiated | 2017-03-03 |
| Classified | 2017-04-18 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2017-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CL, MX, NL, PA, PH, QA, ZA |
| Reason classes | labeling |
| Lot numbers | GC32825 |
| Model numbers | 0270-0429, 0270-0662, 0574-0027 |
Product
It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg). Part Number 0270-0429: GVL 2 Stat (box of 10 Stats). Part Number 0574-0027: GVL 2 Stat (single pouched Stat). Part Number 0270-0662: GlideScope AVL Video Baton 1-2 Kit (where one box of 10, part number 0270-0429), is added as part of the kit.
Reason for recall
Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged with the incorrect size device (GVL 1 Stat (blades)).
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-1852-2017. 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.