Medical Device Recalls
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71 to 73 of 73 Results
510(K) Number: K111825 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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(1) BOX KITDE0143 BYPASS BOX (Item Number: KITDE0143, KITDE0143 BYPASS BOX) (2) BOX ... | 2 | 05/16/2018 | COVIDIEN MEDTRONIC |
(1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) (2)BOX BOX1073180APPE... | 2 | 05/16/2018 | COVIDIEN MEDTRONIC |
(1) BOX 01KBAR006116V PROC BYPASS 01KBAR0061(Item Code 01KBAR006116V PROC BYPAS) (2) BOX 1073076GA... | 2 | 05/16/2018 | COVIDIEN MEDTRONIC |
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