Device recall
Z-0485-2014: FreeStyle Blood Glucose Test Strips; For in vitro diagnostic testing. 50 count…
FDA device recall · Class I · Abbott Diabetes Care, Inc.
Key facts
| Recall number (Z-number) | Z-0485-2014 |
|---|---|
| Recall event | 66886 |
| Product | FreeStyle Blood Glucose Test Strips; For in vitro diagnostic testing. 50 count UPC 6 99073 12050 2; Freestyle Blood Glucose Test Strips; for Institutional Use only 50 count: UPC 6 99073 70792 5 Manufactured by Abbott Diabetes Care Inc. Alameda, CA. The FreeStyle Blood Glucose test strip is intended… |
| Product code | NBW |
| Recalling firm | Abbott Diabetes Care, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 3, 2015 |
| 510(k) numbers | K092602 |
| FEI number | 3002803444 |
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