Device recall
Z-0434-2014: STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code…
FDA device recall · Class III · Advanced Sterilization Products
Key facts
| Recall number (Z-number) | Z-0434-2014 |
|---|---|
| Recall event | 66502 |
| Product | STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code: 13902; STERITITE Mini Mid Size, 3" high, product code: 13903; STERITITE Container Kit, 1/2 size, 4" high, product code: 13904; STERITITE Container Kit, 3/4 size, 4" high, product code: 13905; STERITITE Container Kit… |
| Product code | FRG |
| Recalling firm | Advanced Sterilization Products |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 13, 2014 |
| 510(k) numbers | K023614, K030853, K080558 |
| FEI number | 3003662624 |
At a glance
- 1–9 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