Device recall
Z-0910-2014: MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for…
FDA device recall · Class II · Nipro Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-0910-2014 |
|---|---|
| Recall event | 67152 |
| Product | MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack. Manufactured by: NIPRO DIAGNOSTICS, Fort Lauderdale, FL 33309 U.S.A. Is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm. |
| Product code | NBW |
| Recalling firm | Nipro Diagnostics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 28, 2016 |
| 510(k) numbers | K032657 |
| FEI number | 1000113657 |
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