Device recall
Z-1074-2013: All OneTouch Verio IQ Blood Glucose Meters sold as: Verio IQ System Kits…
FDA device recall · Class I · Lifescan Inc
Key facts
| Recall number (Z-number) | Z-1074-2013 |
|---|---|
| Recall event | 64624 |
| Product | All OneTouch Verio IQ Blood Glucose Meters sold as: Verio IQ System Kits - Meter; Verio IQ Starter kits - Meter; Verio IQ Warranty Meter. Product Usage: The OneTouch VerioIQ Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary… |
| Product code | NBW |
| Recalling firm | Lifescan Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 3, 2015 |
| 510(k) numbers | K1190637 |
| FEI number | 2939301 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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