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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1686-2019 - RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0 2 05/29/2019 FEI # 3005747797
Teleflex Medical
Z-1685-2019 - RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0 2 05/29/2019 FEI # 3005747797
Teleflex Medical
Z-1684-2019 - RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0 2 05/29/2019 FEI # 3005747797
Teleflex Medical
Z-1683-2019 - RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0 2 05/29/2019 FEI # 3005747797
Teleflex Medical
Z-1682-2019 - RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0 2 05/29/2019 FEI # 3005747797
Teleflex Medical
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