Device recall
Z-1852-2017: It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg)…
FDA device recall · Class II · Verathon Inc
Key facts
| Recall number (Z-number) | Z-1852-2017 |
|---|---|
| Recall event | 76642 |
| 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… |
| Product code | CCW |
| Recalling firm | Verathon Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2017 |
| FEI number | 3022472 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database