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Bath, Flotation, Tissue
FDA product code IDY · Class 1 · Pathology
1
Registered devices
1
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-05-01 | Dako North America Inc. | Dako is recalling the PT Link Waterbath because of a possible electrical hazard. Specifically, if the heater pad under the reagent tank becomes wet, it may pr |
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