Device recall
Z-0980-05: LifeScan brand One Touch UltraSmart Meter Owners Booklet AW 060-788-01A; All One…
FDA device recall · Class II · Lifescan Inc
Key facts
| Recall number (Z-number) | Z-0980-05 |
|---|---|
| Recall event | 32360 |
| Product | LifeScan brand One Touch UltraSmart Meter Owners Booklet AW 060-788-01A; All One Touch UltraSmart Meters shipped with OneTouch UltraSmart Owner''s Booklet AW 060-788-01A are affected by this Field Correction. |
| Product code | NBW |
| Recalling firm | Lifescan Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2006 |
| 510(k) numbers | K021819 |
| 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