Aesculap AG
804 devices · 2,193 adverse event reports · 1 deaths reported · 258 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.
- Columbus® CR DD NN230PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AESCULAP FE908KAPPLIER, ANEURYSM CLIP1 report
- S4 SPINAL SYSTEM SW776TORTHOSIS, SPINAL PEDICLE FIXATION1 report
- S4 SPINAL SYSTEM SW777TORTHOSIS, SPINAL PEDICLE FIXATION1 report
- S4 SPINAL SYSTEM SW677TORTHOSIS, SPINAL PEDICLE FIXATION1 report
- CRANIOFIX2 FF492TPLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- ACCULAN 3TI GA672INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- ACCULAN 3TI GB638RINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- NOIR FK916BPUNCH, SURGICAL1 report
- AESCULAP PO889ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- AESCULAP PO887ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- ACTIV L FW953RORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ACTIV L FW954RORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- activL® SW970KPROSTHESIS, INTERVERTEBRAL DISC1 report
- activL® SW972KPROSTHESIS, INTERVERTEBRAL DISC1 report
- activL® SW992KPROSTHESIS, INTERVERTEBRAL DISC1 report
- AESCULAP GA513RMOTOR, SURGICAL INSTRUMENT, PNEUMATIC POWERED1 report
- AESCULAP GF399RAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 report
- AESCULAP FK963RPUNCH, SKULL1 report
- ABC2 FJ910RSCREWDRIVER1 report
- ERGOPLANT DX801RBone mill1 report
- AESCULAP GK375RELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- AESCULAP PO959RELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- NOIR FK984BPUNCH, SURGICAL1 report
- NOIR FK983BPUNCH, SURGICAL1 report
- NEURO-PATCH 1064029DURA SUBSTITUTE1 report
- NEURO-PATCH 1064037DURA SUBSTITUTE1 report
- LYOPLANT 1066064DURA SUBSTITUTE1 report
- AESCULAP FV002RINSTRUMENT, SURGICAL, NON-POWERED1 report
- AESCULAP FV063TShunt, central nervous system and components1 report
- GAV 2.0 FX280TShunt, central nervous system and components1 report
- GAV 2.0 FX216TShunt, central nervous system and components1 report
- GAV 2.0 FX221TShunt, central nervous system and components1 report
- GAV 2.0 FX272TShunt, central nervous system and components1 report
- GAV 2.0 FX231TShunt, central nervous system and components1 report
- GAV 2.0 FX266TShunt, central nervous system and components1 report
- SHUNTASSISTANT 2.0 FX100TShunt, central nervous system and components1 report
- SHUNTASSISTANT 2.0 FX104TShunt, central nervous system and components1 report
- PROGAV 2.0 FX670TShunt, central nervous system and components1 report
- PROGAV 2.0 FX672TShunt, central nervous system and components1 report
- PROGAV 2.0 FX674TShunt, central nervous system and components1 report
- PROGAV 2.0 FX565TShunt, central nervous system and components1 report
- PROGAV 2.0 FX590TShunt, central nervous system and components1 report
- PROGAV 2.0 FX551TShunt, central nervous system and components1 report
- PROGAV 2.0 FX654TShunt, central nervous system and components1 report
- PROGAV 2.0 FX538TShunt, central nervous system and components1 report
- PROGAV 2.0 FX557TShunt, central nervous system and components1 report
- PROGAV 2.0 FX610TShunt, central nervous system and components1 report
- PROGAV 2.0 FX636TShunt, central nervous system and components1 report
- M.BLUE FX805TShunt, central nervous system and components1 report
- M.BLUE FX821TShunt, central nervous system and components1 report
- M.BLUE FX837TShunt, central nervous system and components1 report
- M.BLUE FX840TShunt, central nervous system and components1 report
- M.BLUE FX842TShunt, central nervous system and components1 report
- M.BLUE PLUS FX809TShunt, central nervous system and components1 report
- M.BLUE PLUS FX829TShunt, central nervous system and components1 report
- AESCULAP PL775SUElectrosurgical, cutting & coagulation & accessories1 report
- univation® F NL471PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- univation® F NL473PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- univation® F NL483PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AESCULAP PL531RCLAMP, VASCULAR1 report
- AESCULAP PL548SCLAMP, VASCULAR1 report
- AS Columbus® PS NN173ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® CR/PS NN073ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® CR/PS NN077ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AESCULAP PL541SDEVICE, LOCKING, FOR INTESTINAL CLAMP1 report
- activL® SW888KPROSTHESIS, INTERVERTEBRAL DISC1 report
- AESCULAP SW496TOrthosis, spinal pedicle fixation, for degenerative disc disease1 report
- AESCULAP PO800SUELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- NOIR FK970BPUNCH, SURGICAL1 report
- AESCULAP FS101Neurological stereotaxic Instrument1 report
- CRANIOPLATE FM992TPLATE, BONE1 report
- AS Columbus® REVISION F NR076ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® REVISION F NR073ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® REVISION F NR077ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS NR193ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR194ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR195ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR171ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR178ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR179ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR184ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS NR188ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS NR293ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR295ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR402ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR407ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR409ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR410ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS NR437ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS Columbus® REVISION NR044ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® REVISION NR464ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® REVISION NR465ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® REVISION NR566ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS Columbus® REVISION NR575ZPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- AS ENDURO NB013ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS ENDURO NB015ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- AS ENDURO NB017ZPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Biolox® delta NK560DProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Biolox® delta NK561DProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report