Device recall
Z-0999-2020: ACCU-CHEK AVIVA ASPAC STRIP 50CT- intended for Blood Glucose Monitoring System…
FDA device recall · Class II · Roche Diabetes Care, Inc.
Key facts
| Recall number (Z-number) | Z-0999-2020 |
|---|---|
| Recall event | 84518 |
| Product | ACCU-CHEK AVIVA ASPAC STRIP 50CT- intended for Blood Glucose Monitoring System Catalog Number: 06453970020 |
| Product code | NBW |
| Recalling firm | Roche Diabetes Care, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 8, 2022 |
| FEI number | 3011393376 |
At a glance
- None 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