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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 191 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2610-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F 100CM 3DRC, REF SA63DRCSH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2611-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F 110CM AL20, REF SA6AL20A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2649-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F 3DRIGHT SH .070", REF SA63DRIGHTSH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2660-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F 3DRIGHT, .070", REF SA63DRIGHT. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2639-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL.75 SH, .070", REF SA6AL75SH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2641-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL.75, .070", REF SA6AL75. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2638-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0 SH, .070", REF SA6AL10SH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2624-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0, .070", REF SA6AL10. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2717-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.5 SH, .070", REF SA6AL15SH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2659-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.5, .070", REF SA6AL15. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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