Device recall
Z-1596-05: LifeScan brand OneTouch Ultra Meter - Owner''s Booklet; Product is manufactured…
FDA device recall · Class I · Lifescan Inc
Key facts
| Recall number (Z-number) | Z-1596-05 |
|---|---|
| Recall event | 31815 |
| Product | LifeScan brand OneTouch Ultra Meter - Owner''s Booklet; Product is manufactured and distributed by LifeScan, Inc., 1000 Gibraltar Dr., Milpitas, CA 95037 |
| Product code | NBW |
| Recalling firm | Lifescan Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 29, 2005 |
| 510(k) numbers | K024194 |
| 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