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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 12 Results
510(K) Number: K153440
 
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PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151)... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (U... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
PowerLoc MAX Power Injectable Infusion Set with GuardIVa Antimicrobial Hemostatic Dressing Port Acce... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
PowerLoc MAX Power Injectable Infusion Set; Catalog Numbers 0131910 (UDI 00801741047329), 0131915 (U... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit; Catalog Numbers CPA00001 (UDI 008... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
SafeStep Huber Needle Set AllPoints Port Access System; Catalog Numbers AN152075 (UDI 00801741119484... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
SafeStep Huber Needle Set Port Access Kit; Catalog Numbers PA-0029 (UDI 00801741085482), PA-0029YN (... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
SafeStep Huber Needle Set myPICK Port Access Kit; Catalog Numbers CPA00020A (UDI 00801741129827), CP... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog N... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number CPA00040 (... 2 07/20/2020 FEI # 2243072
Becton Dickinson & Company
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