Device recall
Z-0486-2014: FreeStyle Lite Blood Glucose Test Strips; For in vitro diagnostic testing. 50…
FDA device recall · Class I · Abbott Diabetes Care, Inc.
Key facts
| Recall number (Z-number) | Z-0486-2014 |
|---|---|
| Recall event | 66886 |
| Product | FreeStyle Lite Blood Glucose Test Strips; For in vitro diagnostic testing. 50 count; 100 count Product of Ireland; UPC 6 99073 70819 9; - 50 count UPC 6 99073 70822 9 - 50 count UPC 6 99073 71026 0 - 50 count UPC 6 99073 70827 4 - 100 count Manufactured by Abbott Diabetes Care Inc. Alameda, CA. The… |
| Product code | NBW |
| Recalling firm | Abbott Diabetes Care, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 3, 2015 |
| 510(k) numbers | K092602 |
| FEI number | 3002803444 |
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