Device recall
Z-0514-2009: Quantimetrix Dip and Spin Control Urine Dipstick/Microscopics Control. The…
FDA device recall · Class II · Quantimetrix Corporation
Key facts
| Recall number (Z-number) | Z-0514-2009 |
|---|---|
| Recall event | 48190 |
| Product | Quantimetrix Dip and Spin Control Urine Dipstick/Microscopics Control. The intended use is to validate the performance of the Multistix, Chemstrip, Uriscan, QuickVue, Diascreen and other urinalysis reagent strips, and as a control for confirmatory tests such as Acetest, Clinitest, and Icotest… |
| Product code | JJW |
| Recalling firm | Quantimetrix Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 18, 2009 |
| 510(k) numbers | K874890 |
| FEI number | 2020715 |
At a glance
- 1–9 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