Bard Access Systems, Inc.
1,555 devices · 34,969 adverse event reports · 271 deaths reported · 372 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- PowerPICC SOLO2 Catheter 3295108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000060Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- Hickman 0601790Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000293Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- DuoGlide catheter 5626150CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall2 reports
- Port Access Needle 0141915Set, administration, intravascular1 recall2 reports
- Power-Trialysis Alphacurve catheter 5655200CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall2 reports
- Port Access Needle LH-0037YNSet, administration, intravascular1 recall2 reports
- Port Access Kit PA-0030YNSet, administration, intravascular1 recall2 reports
- PowerPICC HF Catheter 1385118QCatheter,intravascular,therapeutic,long-term greater than 30 days52 reports
- Port Access AN142010GSet, administration, intravascular1 recall2 reports
- Port Access AN162075GSet, administration, intravascular1 recall2 reports
- PowerPICC SOLO CK000524ACatheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC Provena S1193108PDCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000739Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000757Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- Midline Catheter Kit S4254108DGPMidline catheter1 recall2 reports
- Midline Catheter Kit SP4153108DMidline catheter1 recall2 reports
- PowerPICC CK000881Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall2 reports
- PowerPICC CK000991Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall2 reports
- BardPort 0606100PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death51 reports
- PowerPort M.R.I. 1809660PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death51 reports
- PowerPort M.R.I., ChronoFlex 5829502PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death51 reports
- PowerPICC® SV Catheter 3274355Catheter,intravascular,therapeutic,long-term greater than 30 days51 reports
- PowerPICC CK000196Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC Catheter with Sherlock Tip Positioning System (TPS) Stylet 9174118Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Hickman 0601730Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Hickman 0601740Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Groshong 7742000Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- DuoGlide catheter 5625200CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall1 report
- DuoGlide catheter 5626200CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall1 report
- Port Access Kit 2141975Set, administration, intravascular1 recall1 report
- Port Access Needle 0131915Set, administration, intravascular1 recall1 report
- Port Access Needle 0132210Set, administration, intravascular1 recall1 report
- Hickman 0600350Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Port Access Needle LH-0038YNSet, administration, intravascular1 recall1 report
- Port Access Kit PA-0029Set, administration, intravascular1 recall1 report
- Port Access Kit PA-0032Set, administration, intravascular1 recall1 report
- PowerPICC CK000335ACatheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Power-Trialysis Slim-Cath catheter 5865150CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall1 death1 report
- PowerPICC CK000549Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Bard Poly Midline CK000566Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Port Access AN162010Set, administration, intravascular1 recall1 report
- PowerPICC SOLO CK000660Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000589ACatheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC CK000796Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- Midline Catheter Kit S4153108BPMidline catheter1 recall1 report
- PowerPICC Provena S1173108D1Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000285CCatheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000867Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000315ACatheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000267ACatheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000882Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC Provena CK001006Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000937ACatheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000443CCatheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- HemoSplit Long-Term Hemodialysis Catheter 5743690Catheter, hemodialysis, implanted50 reports
- PowerPort ClearVUE 5616000PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death50 reports
- PowerPICC® SV Catheter 3173108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- Hickman 0601710Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- Leonard 0601750Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- Groshong 7741800Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- DuoGlide catheter 5625300CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall0 reports
- DuoGlide catheter 5626120CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall0 reports
- DuoGlide catheter 5626240CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall0 reports
- Port Access Kit 2131910Set, administration, intravascular1 recall0 reports
- Port Access Kit 2131915Set, administration, intravascular1 recall0 reports
- Port Access Kit 2131975Set, administration, intravascular1 recall0 reports
- Port Access Kit 2132015Set, administration, intravascular1 recall0 reports
- Port Access Kit 2132210Set, administration, intravascular1 recall0 reports
- Port Access Kit 2132275Set, administration, intravascular1 recall0 reports
- Port Access Kit 2141910Set, administration, intravascular1 recall0 reports
- Port Access Kit 2141915Set, administration, intravascular1 recall0 reports
- Port Access Kit 2142010Set, administration, intravascular1 recall0 reports
- Port Access Kit 2142015Set, administration, intravascular1 recall0 reports
- Port Access Kit 2142210Set, administration, intravascular1 recall0 reports
- Port Access Kit 2142215Set, administration, intravascular1 recall0 reports
- Port Access Kit 2142275Set, administration, intravascular1 recall0 reports
- Aspira Dressing Kit 4991503APPARATUS, SUCTION, PATIENT CARE1 recall0 reports
- Niagara catheter 5766200CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall0 reports
- Port Access Needle 0132015Set, administration, intravascular1 recall0 reports
- Port Access Needle 0132215Set, administration, intravascular1 recall0 reports
- Port Access Needle 0142215Set, administration, intravascular1 recall0 reports
- Power-Trialysis Alphacurve catheter 5655150CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall0 reports
- Power-Trialysis Alphacurve catheter 5655240CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall0 reports
- Port Access Needle LH-0036Set, administration, intravascular1 recall0 reports
- Port Access Needle LH-0036YNSet, administration, intravascular1 recall0 reports
- Port Access Needle LH-0040Set, administration, intravascular1 recall0 reports
- Port Access Needle LH-0040YNSet, administration, intravascular1 recall0 reports
- Power-Trialysis catheter 5615240CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall0 reports
- Port Access Kit PA-0030Set, administration, intravascular1 recall0 reports
- Port Access Kit PA-0032YNSet, administration, intravascular1 recall0 reports
- Port Access Kit PA-0033Set, administration, intravascular1 recall0 reports
- Port Access Kit PA-0033YNSet, administration, intravascular1 recall0 reports
- Port Access Kit PA-0034Set, administration, intravascular1 recall0 reports
- Port Access Kit PA-0034YNSet, administration, intravascular1 recall0 reports
- Port Access Kit PA-0036Set, administration, intravascular1 recall0 reports
- Port Access Kit PA-0038Set, administration, intravascular1 recall0 reports
- Port Access Kit PA-0038YNSet, administration, intravascular1 recall0 reports
- Port Access Kit PA-0031GSet, administration, intravascular1 recall0 reports