Device recall
Z-1912-2009: Broselow/Hinkle Pediatric Emergency System; Contents: 1 15 Ga Adjustable Length…
FDA device recall · Class II · Vital Signs Inc
Key facts
| Recall number (Z-number) | Z-1912-2009 |
|---|---|
| Recall event | 52694 |
| Product | Broselow/Hinkle Pediatric Emergency System; Contents: 1 15 Ga Adjustable Length Sternal/Iliac aspiration Needle; 1 Extension Set, Sterile. Equipment Color Zone: Green, Single Patient use, INTRAOSSEUS Module, Product # 7700GIO, Vital Signs, Totowa, NJ. The Broselow/Hinkle Pediatric Emergency System… |
| Product code | GAA |
| Recalling firm | Vital Signs Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2012 |
| FEI number | 2242551 |
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