Device recall
Z-2881-2020: Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC…
FDA device recall · Class II · Klarity Medical Products LLC
Key facts
| Recall number (Z-number) | Z-2881-2020 |
|---|---|
| Recall event | 86146 |
| Product | Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product Usage: To be used by trained medical professionals for the stable support and positioning of patients undergoing external beam radiation therapy treatment in a clinic or hospital… |
| Product code | IYE |
| Recalling firm | Klarity Medical Products LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 19, 2020 |
| 510(k) numbers | K132124 |
| FEI number | 3001236129 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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