Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 10/09/2015 510(K) Number: K915285 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Skytron Infinity Series surgical light, 5 bulbs in 1 - 22' diameter lighthead, Manufactured by Dai-i... | 2 | 02/22/2007 | Skytron, Div. The KMW Group, Inc |
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