Device recall
Z-0939-2012: Broselow/Hinkle Pediatric Emergency System Vital Signs Inc. 20 Campus Road…
FDA device recall · Class II · Vital Signs Devices, a GE Healthcare Company
Key facts
| Recall number (Z-number) | Z-0939-2012 |
|---|---|
| Recall event | 60016 |
| Product | Broselow/Hinkle Pediatric Emergency System Vital Signs Inc. 20 Campus Road Totowa, NJ 07512 USA The system supplies you with all the information and equipment needed for a young patients' emergency resuscitation requirements, all contained in a color coded, easy-to-use kit |
| Product code | OGL |
| Recalling firm | Vital Signs Devices, a GE Healthcare Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 15, 2013 |
| FEI number | 2242551 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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