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.
- PowerPort ClearVUE 5676301PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall1 death12 reports
- PowerPICC Provena SOLO S1295108FD3Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports
- PowerPICC SOLO CK000930Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall12 reports
- Midline Catheter Kit S4254108BDPMidline catheter1 recall11 reports
- PowerPICC Provena S1193108D4Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall11 reports
- PowerPICC Provena S1173108D5Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall11 reports
- PowerPICC Provena SOLO S1295108FD5Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall11 reports
- Site~Rite 8 Ultrasound System 9770603RTransducer, ultrasonic, diagnostic61 reports
- PowerPICC SOLO2 Catheter 3194118Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall10 reports
- PowerPICC SOLO2 Catheter 3194155Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall10 reports
- Navarre NBD8CATHETER, BILIARY, DIAGNOSTIC60 reports
- Port Access Needle 0132275Set, administration, intravascular1 recall10 reports
- Midline Catheter Kit P4154108Midline catheter1 recall10 reports
- Peripheral Catheter Insertion Kit F318108PTCatheter,intravascular,therapeutic,short-term less than 30 days60 reports
- PowerPICC® Catheter 3174108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall9 reports
- Port Access Needle LH-0034YNSet, administration, intravascular1 recall9 reports
- Port Access Kit PA-0031Set, administration, intravascular1 recall9 reports
- Sherlock 9770131RCatheter,intravascular,therapeutic,long-term greater than 30 days59 reports
- AccuCath Ace AC1202252Catheter, intravascular, therapeutic, short-term less than 30 days59 reports
- BD Prevue II Peripheral Vascular Access System 9770700Transducer, ultrasonic, diagnostic59 reports
- PowerPort M.R.I., ChronoFlex 1808062PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR4 deaths58 reports
- Hickman 0601630Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall8 reports
- Hickman 0601700Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall8 reports
- Hickman 0600310Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall8 reports
- Port Access Needle LH-0030YNSet, administration, intravascular1 recall8 reports
- Power-Trialysis catheter 5615150CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall2 deaths8 reports
- Port Access Needle SHG19-75Set, administration, intravascular58 reports
- Port Access AN142075Set, administration, intravascular1 recall8 reports
- Peripheral Catheter Insertion Kit ST018101DMidline catheter1 recall8 reports
- Midline Catheter Kit S4254108DMidline catheter1 recall8 reports
- PowerPICC Provena S1275108FD2Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall8 reports
- PowerPICC SOLO2 Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet 1194108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- Groshong NXT Catheter 7957505Catheter,intravascular,therapeutic,long-term greater than 30 days57 reports
- Hickman 0601690Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- Port Access Kit PA-0031YNSet, administration, intravascular1 recall7 reports
- Site-Rite 9770086Transducer, ultrasonic, diagnostic57 reports
- Midline Catheter Kit P4254108DMidline catheter1 recall7 reports
- PowerPICC Provena S3274108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC CK000632BCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC 1174108D1Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC Provena S1385108D3Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC Provena S1193108D3Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall7 reports
- PowerPICC CK000986Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall7 reports
- PowerPICC SOLO2 Catheter with Sherlock Tip Location System (TLS) Stylet 9194108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall6 reports
- Groshong NXT Catheter 7857505Catheter,intravascular,therapeutic,long-term greater than 30 days56 reports
- Broviac 0600120Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall6 reports
- Port Access Needle LH-0034Set, administration, intravascular1 recall6 reports
- PowerPICC Provena S1275108FD3Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall6 reports
- PowerPICC® Catheter 3174108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC® Catheter 3275108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC Catheter with Sherlock Tip Location System (TLS) Stylet 9174108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- Broviac 0601600Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- Site-Rite 900013B01Transducer, ultrasonic, diagnostic55 reports
- Port Access Needle LH-0039Set, administration, intravascular1 recall5 reports
- PowerPort ClearVUE 1676301PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall5 reports
- PowerPICC SOLO CK000687Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- AccuCath Ace AC1182250Catheter, intravascular, therapeutic, short-term less than 30 days55 reports
- PowerMidline CK000727Midline catheter1 recall5 reports
- PowerPICC CK000819Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC CK000897Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- PowerPICC Provena CK000988Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- PowerPort ClearVUE 1606052PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR54 reports
- PowerPICC Catheter 3175155Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- Poly RadPICC Catheter 3164155Catheter,intravascular,therapeutic,long-term greater than 30 days54 reports
- PowerPICC Catheter with Sherlock Tip Positioning System (TPS) Stylet 9174108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- Aspira Drainage Kit 4992301CATHETER, PERITONEAL, LONG-TERM INDWELLING1 recall4 reports
- Port Access Needle 0141910Set, administration, intravascular1 recall4 reports
- Port Access Needle 0142015Set, administration, intravascular1 recall4 reports
- Port Access Needle 0142210Set, administration, intravascular1 recall4 reports
- Broviac 0600100Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- Port Access Needle LH-0038Set, administration, intravascular1 recall4 reports
- Port Access Kit PA-0029YNSet, administration, intravascular1 recall4 reports
- Port Access AN132075Set, administration, intravascular1 recall4 reports
- PowerPICC CK000677Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerMidline CK000729Midline catheter1 recall4 reports
- PowerPICC Provena SOLO S1295108FD1Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC Provena SOLO S1395108D1Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC Provena S1385108D2Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC SOLO CK000900Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- PowerPICC Provena CK000883Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- PowerPICC Provena CK000886Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- PowerPICC SOLO CK001027Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- X-Port isp M.R.I., ChronoFlex 0607540PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death53 reports
- PowerPICC Catheter 3174135Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC SOLO2 Catheter 3194135Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000724TUBES, GASTROINTESTINAL (AND ACCESSORIES)53 reports
- DuoGlide catheter 5625150CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall3 reports
- Port Access Kit 2132075Set, administration, intravascular1 recall3 reports
- Niagara catheter 5593200CATHETER, HEMODIALYSIS, NON-IMPLANTED53 reports
- PowerPICC CK000411Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC CK000513ACatheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- Port Access AN162075Set, administration, intravascular1 recall3 reports
- Bard Poly Midline CK000495ACatheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- Midline Catheter Kit P4254108Midline catheter1 recall1 death3 reports
- PowerPICC SOLO CK000501ACatheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC CK000870ACatheter, intravascular, therapeutic, long-term greater than 30 days1 recall3 reports
- Midline Catheter Kit SP4153108DGMidline catheter1 recall3 reports
- PowerPICC Sherlock 3CG CK000668BCatheter, intravascular, therapeutic, long-term greater than 30 days1 recall3 reports
- PowerPort M.R.I., Groshong 4808560PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death52 reports
- PowerPICC SOLO2 Catheter 3194108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports