Device recall
Z-0934-2008: Inotech brand Heparin Adsorbant, Catalog #: HA-1, in 10mm x 75mm polystyrene…
FDA device recall · Class II · Inotech Biosystems Intl., Inc
Key facts
| Recall number (Z-number) | Z-0934-2008 |
|---|---|
| Recall event | 45407 |
| Product | Inotech brand Heparin Adsorbant, Catalog #: HA-1, in 10mm x 75mm polystyrene tubes, each containing 70mg of Heparin Adsorbent, 10 tubes per foil lined pouch, 10 foil pouches/box, Inotech Biosystems International, Inc., Rockville, MD 20855 |
| Product code | JPA |
| Recalling firm | Inotech Biosystems Intl., Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 7, 2012 |
| 510(k) numbers | K870771 |
| FEI number | 1832416 |
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