Medical Device Recalls
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1 result found
Recall Number: Z-2691-2016 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| HexaPOD evo RT System Product Usage: The intended use of the device is the control of accurate p... | 2 | 08/30/2016 |
FEI # 1037831 Elekta, Inc. |
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