Patient reported that huber powerloc needle line is splitting.She switched to safestep, which was also splitting.Then, a recall on these products was released.The patient developed swelling and a lump at her port site.She then developed a fever and was hospitalized.Her port is being removed and a midline iv will be placed so that she can receive iv antibiotics.More information to follow after she is released from the hospital and we can get a full timeline of events and lot numbers.Huber powerloc 22gx1 (lot # ascyf018, ascyf019, asczf026, asdrf047, asdrf048, asdrf049, asdrf050); huber safestep 22x0.5 (lot # ascyf013, ascyf014, asczf029, ascvf034,ascvf035, ascvf038, ascvf042); huber safestep 22x1 (lot # asdnf034, asdnf049, asdnf055, asdpf015, asdpf017, asdpf021, asdpf024, asdpf025, asdpf026, asdqf017, asdrf066, asduf120, asdvf004, asdvf009, asdvf013, asdvf016, asdvf025).Fda safety report id# (b)(4).
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