Device recall
Z-0231-2019: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx…
FDA device recall · Class II · Ecolab Inc
Key facts
| Recall number (Z-number) | Z-0231-2019 |
|---|---|
| Recall event | 81244 |
| Product | Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system Distribute by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to cover/wrap various surgical and/or… |
| Product code | PUI |
| Recalling firm | Ecolab Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2021 |
| FEI number | 3014342658 |
At a glance
- None 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