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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 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-2572-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, AR2.0 SH, 100CM.070", REF SA6AR20SH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2573-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP0.5, 100CM.070", REF SA6CHAMP05. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2574-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP0.5 SH, 100CM.070", REF SA6CHAMP05SH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2575-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP2.0, 55CM.070", REF SA6CHAMP20K. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2576-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, EBU3.5, 110CM.070", REF SA6EBU35A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2577-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, EBU3.5, 90CM.070", REF SA6EBU35D. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2578-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, EBU4.0, 110CM.070", REF SA6EBU40A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2579-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, FL4.0, 100CM.070", REF SA6FL40. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2580-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, FL4.0 SH, 100CM, 070", REF SA6FL40SH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2581-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, HSI, 100CM, 070", REF SA6HSI. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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