Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K140658 |
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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 ThermoGard® Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Numb... | 2 | 08/19/2016 |
FEI # 1317214 Conmed Corporation |
| Adult ThermoGard® Dual Dispersive Electrodes (for patients >15 kg.), No Cable, Catalog Number 51-741... | 2 | 08/19/2016 |
FEI # 1317214 Conmed Corporation |
| Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.), use with the Birtcher Pad Sensing Syst... | 2 | 08/19/2016 |
FEI # 1317214 Conmed Corporation |
| Adult Dual Dispersive Electrodes (for patients >15 kg.), use with the Birtcher Pad Sensing System (P... | 2 | 08/19/2016 |
FEI # 1317214 Conmed Corporation |
| Pediatric ThermoGard® Dual Dispersive Electrodes (for patients 5-15 kg.), 10' (3.05m) Cable, Catalog... | 2 | 08/19/2016 |
FEI # 1317214 Conmed Corporation |
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