Recall Z-1156-2021— Hamilton Co
Class II · Ongoing
Class II FDA medical device recall by Hamilton Co, initiated 2021-01-15. FDA's recall record names no specific 510(k) clearance for this event. Product: HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no condensation. REF 19903400. Reason: There is a risk that the device can start a fire if flammable liquids contact and enter the device..
- Recalling firm
- Hamilton Co
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2021-01-15
- Firm location
- Reno, NV, United States
Product description
HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no condensation. REF 19903400
Reason for recall
There is a risk that the device can start a fire if flammable liquids contact and enter the device.
Data sourced from openFDA. This site is unofficial and independent of the FDA.