Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K093914 |
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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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UNI-CP, Model Numbers: 330021S, 330023S, 330025S, 330030S, 330025S, 30030S, 330217S, 330220S, 330225... | 2 | 07/16/2018 | NewDeal SA |
ADVANSYS TTC, Model Numbers: 181011S, 181012S, 181013S, 181014S, 181001S, 181002S, 181003S & 181004... | 2 | 07/16/2018 | NewDeal SA |
TIBIAXYS, Model Numbers: 150010S, 150020S, 150030S, 150040S, 150120S, 150110S, 150130S, 150200S, 1... | 2 | 07/16/2018 | NewDeal SA |
Large QWIX, Model Numbers: 111740S, 111745S, 111750S, 111755S, 111760S, 111765S, 111770S, 111775S,... | 2 | 07/16/2018 | NewDeal SA |
ADVANSYS MLP/DLP, Model Numbers: 181051S, 181052S, 181041S, 181042S, 181031S, 181032S, 181033S, 1810... | 2 | 07/16/2018 | NewDeal SA |
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