Device recall
Z-0398-03: SureStep 50 Test Strips, For the measurement of glucose in whole blood, Two…
FDA device recall · Class II · River City Drug
Key facts
| Recall number (Z-number) | Z-0398-03 |
|---|---|
| Recall event | 25193 |
| Product | SureStep 50 Test Strips, For the measurement of glucose in whole blood, Two bottles of 25 Test Srips, LIFESCAN, a Johnson & Johnson Company, Milpitas, CA 95035, USA, Lot: E-169380A, Exp: 2003-01. |
| Product code | JJQ |
| Recalling firm | River City Drug |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 7, 2005 |
| FEI number | 3003714050 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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