Device recall
Z-0777-2019: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage…
FDA device recall · Class III · Riverpoint Medical, LLC
Key facts
| Recall number (Z-number) | Z-0777-2019 |
|---|---|
| Recall event | 81935 |
| Product | RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage: The Riverpoint Brachytherapy Grid is used during Brachytherapy procedures to assist with the precise insertion of the needle or other probes. The Riverpoint Brachytherapy Grid is placed against the skin of the patient to… |
| Product code | IWJ |
| Recalling firm | Riverpoint Medical, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 15, 2019 |
| FEI number | 3006981798 |
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