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U.S. Department of Health and Human Services

Medical Device Recalls
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51 to 56 of 56 Results
Related Medical Device Recalls
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Z-2303-2017 - ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit The large-bore multiple-lumen catheter permits venous access to the central circulation for rapid fluid administration. It may be inserted into the ju... 2 06/06/2017 FEI # 3015859709
Arrow International Inc
Z-2304-2017 - Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5-8 Fr. Catheters The A... 2 06/06/2017 FEI # 3015859709
Arrow International Inc
Z-2305-2017 - ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of diseases or conditions req... 2 06/06/2017 FEI # 3015859709
Arrow International Inc
Z-2306-2017 - Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions for High Volume Infusions The Arrow(r) CVC is indi... 2 06/06/2017 FEI # 3015859709
Arrow International Inc
Z-2307-2017 - ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of d... 2 06/06/2017 FEI # 3015859709
Arrow International Inc
Z-2254-2017 - ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R) permits venous access an... 2 06/06/2017 FEI # 3015859709
Arrow International Inc
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