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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 12 of 12 Results
Related Medical Device Recalls
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Z-0998-2018 - AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Arrow® CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring c... 2 03/14/2018 FEI # 3015859709
Arrow International Inc
Z-1003-2018 - AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Arrow® CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring c... 2 03/14/2018 FEI # 3015859709
Arrow International Inc
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