Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110104 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Blanketrol II Hyper-Hypothermia System, Models 222R and 222S - Product Usage: The system is compose... | 2 | 11/18/2019 | Cincinnati Sub-Zero Products LLC, a Gentherm Company |
115 V Blanketrol II, Model 222S Hyper-Hypothermia System . Used to lower or to raise a patients tem... | 2 | 06/10/2014 | Cincinnati Sub-Zero Products Inc |
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