Device recall
Z-2335-2008: Radiation Reduction Gloves, sterile, Latex-free, Catalog No. SSR1-7.0, SSR1-7.5…
FDA device recall · Class II · Integra Pain Management
Key facts
| Recall number (Z-number) | Z-2335-2008 |
|---|---|
| Recall event | 48971 |
| Product | Radiation Reduction Gloves, sterile, Latex-free, Catalog No. SSR1-7.0, SSR1-7.5, SSR1-8.0, Integra Pain Management, 3395 West 1820 South, Salt Lake City, Utah 84104. |
| Product code | LZC |
| Recalling firm | Integra Pain Management |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2008 |
| FEI number | 1000138491 |
At a glance
- None 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