Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K942599 |
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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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WarmAir 135 Thermal Regulating System. Catalog Numbers: 86186-115 V, 06186-115 V (sold in the U.S.)... | 2 | 10/29/2009 | Cincinnati Sub-Zero Products Inc |
Warm Air Model 135 Warming Units. | 2 | 12/30/2004 | Cincinnati Sub-Zero Products |
FilteredFlo® Cardiac Blanket. The device is used to distribute heated air around a patient (for p... | 2 | 02/04/2010 | Cincinnati Sub-Zero Products Inc |
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