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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 191 Results
Related Medical Device Recalls
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Product Description
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Z-2632-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F JR5.0, .070", REF SA6JR50. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2633-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU4.5, .070", REF SA6EBU45. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2634-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F SL3.5, .070", REF SA6SL35. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2635-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC3.0 .070", REF SA6MAC30. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2636-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F M RESS, .070", REF SA6MRESS. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2637-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F SCR4.0 SH, .070", REF SA6SCR40SH. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2638-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0 SH, .070", REF SA6AL10SH. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2639-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL.75 SH, .070", REF SA6AL75SH. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2640-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU5.0, .070", REF SA6EBU50. for cardiovascular use 1 10/01/2019 Medtronic Vascular
Z-2641-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F AL.75, .070", REF SA6AL75. for cardiovascular use 1 10/01/2019 Medtronic Vascular
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