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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 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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Recalling Firm
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Z-0742-03 - Tandem-Cath Hemodialysis Cuffed Catheter with side holes 10 Fr 19 cm Arterial Cuff/22cm Venous Cuff Code #: 8888-219226 2 04/18/2003 Tyco Healthcare/Kendall
Z-0743-03 - Tandem-Cath Hemodialysis Cuffed Catheter with side holes 10 Fr 23 cm Arterial Cuff/26cm Venous Cuff Code #: 8888-223266 2 04/18/2003 Tyco Healthcare/Kendall
Z-0747-03 - Tandem-Cath Hemodialysis Cuffed Catheter with no side holes 10 Fr 28 cm Arterial Cuff/31cm Venous Cuff Code #: 8888-228310 2 04/18/2003 Tyco Healthcare/Kendall
Z-0745-03 - Tandem-Cath Hemodialysis Cuffed Catheter with no side holes 10 Fr 19 cm Arterial Cuff/22cm Venous Cuff Code #: 8888-219220 2 04/18/2003 Tyco Healthcare/Kendall
Z-0746-03 - Tandem-Cath Hemodialysis Cuffed Catheter with no side holes 10 Fr 23 cm Arterial Cuff/26cm Venous Cuff Code #: 8888-223260 2 04/18/2003 Tyco Healthcare/Kendall
Z-0744-03 - Tandem-Cath Hemodialysis Cuffed Catheter with side holes 10 Fr 28 cm Arterial Cuff/31 cm Venous Cuff Code #: 8888-228316 2 04/18/2003 Tyco Healthcare/Kendall
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