Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K011693 |
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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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Trumpf Ceiling Mounted Surgical Lighting Systems,Helion/Xenion S/M/L, User Manual #1441784. The T... | 2 | 08/07/2015 | Trumpf Medical Systems, Inc. |
Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of t... | 2 | 12/12/2013 | Trumpf Medical Systems, Inc. |
Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to... | 2 | 10/18/2012 | Trumpf Medical Systems, Inc. |
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