Device recall
Z-2220-2017: Large Stealth Chamber, Catalog Numbers: DS50-001-XL-T, DS50-002-XL-T…
FDA device recall · Class II · Iba Dosimetry
Key facts
| Recall number (Z-number) | Z-2220-2017 |
|---|---|
| Recall event | 77301 |
| Product | Large Stealth Chamber, Catalog Numbers: DS50-001-XL-T, DS50-002-XL-T, DS50-003-XL-T, DS50-102-XL-T, DS50-103-XL-T |
| Product code | IYE |
| Recalling firm | Iba Dosimetry |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2018 |
| 510(k) numbers | K945321 |
| FEI number | 3001238439 |
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