Device recall
Z-0875-2008: Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sate Dry Acid Concentrate…
FDA device recall · Class II · Rockwell Medical Technologies, Inc
Key facts
| Recall number (Z-number) | Z-0875-2008 |
|---|---|
| Recall event | 46267 |
| Product | Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sate Dry Acid Concentrate DR-240); 1 quart (0.95 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051. |
| Product code | KPO |
| Recalling firm | Rockwell Medical Technologies, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 31, 2008 |
| 510(k) numbers | K981003 |
| FEI number | 3003463852 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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