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U.S. Department of Health and Human Services

Medical Device Recalls

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31 to 40 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-2592-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JR4.0, 110CM, 070", REF SA6JR40A. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2593-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JR4.0, 90CM, 070", REF SA6JR40D. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2594-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, JR4.0, 55CM, 070", REF SA6JR40K. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2595-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, LCB SH, 90CM, 070", REF SA6LCBSHD. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2596-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, MB1, 90CM, 070", REF SA6MB1D. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2597-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, MP1, 55CM, 070", REF SA6MP1K. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2598-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, MPH, 55CM, 070", REF SA6MPHK. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2599-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, NOTO, 100CM, 070", REF SA6NOTO. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2600-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, NOTO SH, 100CM, 070", REF SA6NOTOSH. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2601-2019 - SHERPA NX ACTIVE GUIDING CATHETER, 6F, PK1, 47CM, 070", REF SA6PK1W. for cardiovascular use 1 10/01/2019 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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