Device recall
Z-0484-2016: 1 Step 12 Panel Cup, Item No. NBCA-12M-W
FDA device recall · Class III · Ameditech Inc
Key facts
| Recall number (Z-number) | Z-0484-2016 |
|---|---|
| Recall event | 72651 |
| Product | 1 Step 12 Panel Cup, Item No. NBCA-12M-W |
| Product code | JXM |
| Recalling firm | Ameditech Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 9, 2016 |
| 510(k) numbers | K052115 |
| FEI number | 3003789989 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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