Device recall
Z-0606-2018: Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog 200265…
FDA device recall · Class II · Gibson Laboratories LLC
Key facts
| Recall number (Z-number) | Z-0606-2018 |
|---|---|
| Recall event | 78731 |
| Product | Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog 200265 Intended for identification of the systemic fungal pathogens. |
| Product code | LSI |
| Recalling firm | Gibson Laboratories LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2018 |
| FEI number | 1050138 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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