fda
4 records
FDA Device Recall: TIBIAXYS, Model Numbers: 150010S, 150020S, 150030S, 150040S, 150120S, 150110S,
2018-07-25
Class II — Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.
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FDA Device Recall: UNI-CP, Model Numbers: 330021S, 330023S, 330025S, 330030S, 330025S, 30030S, 3302
2018-07-25
Class II — Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.
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FDA Device Recall: ADVANSYS MLP/DLP, Model Numbers: 181051S, 181052S, 181041S, 181042S, 181031S, 18
2018-07-25
Class II — Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.
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FDA Device Recall: Large QWIX, Model Numbers: 111740S, 111745S, 111750S, 111755S, 111760S, 111765
2018-07-25
Class II — Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.
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irs_exempt
1 records
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