Medical Device Recalls
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1 result found
Recall Number: Z-2598-2016 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Adult Dual Dispersive Electrodes (for patients >15 kg.), use with the Birtcher Pad Sensing System (P... | 2 | 08/19/2016 |
FEI # 1317214 Conmed Corporation |
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