Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K103318 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 731 Series Ventilators running software version 05.20.00 The devices in the ZOLL ventilator are ... | 2 | 03/01/2018 | ZOLL Medical Corporation |
| Model 731 EMV+ Uni-Vent, Impact Instrumentation Inc., 27 Fairfield Place, West Caldwell NJ 07006. In... | 3 | 08/07/2012 | Impact Instrumentation, Inc. |
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