Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K002280 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602... | 2 | 03/24/2018 | ConMed Corporation |
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602... | 2 | 03/24/2018 | ConMed Corporation |
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, ZOLL® Connector, REF/Catalog Number 2602Z Indicat... | 2 | 03/24/2018 | ConMed Corporation |
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602... | 2 | 03/24/2018 | ConMed Corporation |
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control® Quik-Combo" Connector, REF/Catalog Nu... | 2 | 03/24/2018 | ConMed Corporation |
MINI PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2602H, Rx ONLY --- COMPARABLE TO PHILI... | 1 | 12/04/2014 | ConMed Corporation |
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