Medical Device Recalls
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1 result found
Recall Date to: 11/01/2014 PMA Number: P010032/S014 |
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Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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Eon (Model 3716) IPG is a dual channel; 8-contact receiver designed to be connected to 4, 8, or 16 e... | 2 | 08/28/2012 | Advanced Neuromodulation Systems Inc. |
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