Device recall
Z-1070-2009: OneTouch SureStep Test Strips, Part numbers 020-052-01 and 010-359-04, for use…
FDA device recall · Class II · Lifescan Inc
Key facts
| Recall number (Z-number) | Z-1070-2009 |
|---|---|
| Recall event | 50471 |
| Product | OneTouch SureStep Test Strips, Part numbers 020-052-01 and 010-359-04, for use with SureStep brand Blood Glucose Meters, manufactured by LifeScan Inc., Milpitas, CA |
| Product code | NBW |
| Recalling firm | Lifescan Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 6, 2010 |
| 510(k) numbers | K022724 |
| 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