Device recall
Z-0753-2017: Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.
FDA device recall · Class III · Ecolab Inc
Key facts
| Recall number (Z-number) | Z-0753-2017 |
|---|---|
| Recall event | 75826 |
| Product | Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only. |
| Product code | KKX |
| Recalling firm | Ecolab Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 21, 2019 |
| 510(k) numbers | K882724 |
| FEI number | 1000289767 |
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