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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 of 191 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-2582-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, HSI SH, 100CM, 070", REF SA6HSISH . for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2583-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA, 100CM, 070", REF SA6IMA. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2584-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA, 90CM, 070", REF SA6IMAD . for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2585-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA SH, 100CM, 070", REF SA6IMASH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2586-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA SH, 60CM, 070", REF SA6IMASHJ. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2587-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JCR4.0, 100CM, 070", REF SA6JCR40. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2588-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JL3.5, 110CM, 070", REF SA6JL35A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2589-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JL4.0, 110CM, 070", REF SA6JL40A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2590-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JL4.0, 90CM, 070", REF SA6JL40D. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2591-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JL5.0, 110CM, 070", REF SA6JL50A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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