Device recall
Z-2330-2021: AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM…
FDA device recall · Class II · PROCEPT BIOROBOTICS CORPORATION
Key facts
| Recall number (Z-number) | Z-2330-2021 |
|---|---|
| Recall event | 88337 |
| Product | AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System. |
| Product code | PZP |
| Recalling firm | PROCEPT BIOROBOTICS CORPORATION |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K202961 |
| FEI number | 3027788423 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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