Device recall
Z-2221-2017: Urea Base Agar, Acumedia PN 7226 Urea Agar Base is used with agar for the…
FDA device recall · Class III · Acumedia Manufacturers, Inc.
Key facts
| Recall number (Z-number) | Z-2221-2017 |
|---|---|
| Recall event | 77276 |
| Product | Urea Base Agar, Acumedia PN 7226 Urea Agar Base is used with agar for the differentiation of microorganisms on the basis of urease production |
| Product code | JSI |
| Recalling firm | Acumedia Manufacturers, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 2, 2017 |
| FEI number | 1120041 |
At a glance
- None 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