Device recall
Z-0714-2020: Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters…
FDA device recall · Class II · Alliance Tech Medical, Inc
Key facts
| Recall number (Z-number) | Z-0714-2020 |
|---|---|
| Recall event | 83830 |
| Product | Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed bag printed with the part number, 100 filters/box, for single patient use, latex free, box of 100 Reorder Numbers: 5553100 (single filter reorder no. 5553000), 5554100 (single filter… |
| Product code | CAH |
| Recalling firm | Alliance Tech Medical, Inc |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K043148 |
| FEI number | 3004476631 |
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