Device recall
Z-0007-2017: 0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacteria and…
FDA device recall · Class I · Baxter Corporation Englewood
Key facts
| Recall number (Z-number) | Z-0007-2017 |
|---|---|
| Recall event | 75031 |
| Product | 0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacteria and particulate filter for aqueous solutions. It attaches to a standard Baxter Pharmacy Pump Tube Set. |
| Product code | LHI |
| Recalling firm | Baxter Corporation Englewood |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 26, 2017 |
| 510(k) numbers | K900585 |
| FEI number | 1419106 |
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