Home › Device types › DGW
System, Test, Hypersensitivity Pneumonitis
FDA product code DGW · Class 2 · Immunology
0
Registered devices
1
Adverse events
2
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-10-25 | Greer Laboratories, Inc. | The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to a potential false-negative result interp |
| 2022-10-25 | Greer Laboratories, Inc. | The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to a potential false-negative result interp |
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