Brand

Aesculap, Inc. Recalls

28 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Aesculap, Inc..

28Total Recalls
0Critical
988,132Units Affected
Jan 15, 2026Most Recent
All Recalls

Every Aesculap, Inc. Recall

Sorted by most recent. Click any recall for full details.

28 recalls
High RiskFDA
Aesculap Inc
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product...
Medical Devices·126 affected·Jan 15, 2026
High RiskFDA
Aesculap Inc
Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Produc...
Medical Devices·26 affected·Sep 24, 2025
High RiskFDA
Aesculap Inc
Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A Product Descr...
Medical Devices·155 affected·Sep 24, 2025
High RiskFDA
Aesculap Inc
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Fo...
Surgical Devices·47,078 affected·Jan 31, 2025
High RiskFDA
Aesculap Inc
Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hys...
Surgical Devices·19,979 affected·Jan 31, 2025
High RiskFDA
Aesculap Inc
Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2) REF BH104R, Hartmann Mosquito FCSDEL ...
Surgical Devices·917,965 affected·Jan 31, 2025
High RiskFDA
Aesculap Inc
Aeos Robotic Digital Microscope, Product Code: PV010
Medical Devices·19 affected·May 13, 2024
High RiskFDA
Aesculap Inc
DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
Medical Devices·18 affected·Jan 9, 2024
High RiskFDA
Aesculap Inc
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.
Medical Devices·6 affected·Jan 9, 2024
High RiskFDA
Aesculap Inc
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.
Medical Devices·6 affected·Jan 9, 2024
High RiskFDA
Aesculap Inc
MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"
Medical Devices·60 affected·Dec 29, 2023
High RiskFDA
Aesculap Inc
MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";
Medical Devices·53 affected·Dec 29, 2023
High RiskFDA
Aesculap, Inc.
Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicat...
Medical Devices·1,232 affected·Nov 30, 2015
High RiskFDA
Aesculap, Inc.
Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the ...
Medical Implants·37 affected·Nov 10, 2015
High RiskFDA
Aesculap, Inc.
Flexible Drill; SJ723R; NON STERILE; B Braun Aesculap; Aesculap AG These instruments are intended for use during the implantati...
Medical Implants·13 affected·Nov 10, 2015
High RiskFDA
Aesculap, Inc.
S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tig...
Medical Devices·10 affected·Jul 7, 2015
High RiskFDA
Aesculap, Inc.
Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ...
Medical Devices·772 affected·Dec 17, 2014
RecallFDA
Aesculap, Inc.
Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ve...
Medical Devices·4 affected·Nov 11, 2014
High RiskFDA
Aesculap, Inc.
Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Surgical Suture, additional label affixed on the bo...
Surgical Devices·11 affected·Jun 13, 2014
High RiskFDA
Aesculap, Inc.
Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is intended to shut cere...
Surgical Devices·48 affected·Apr 21, 2014
High RiskFDA
Aesculap, Inc.
Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut cerebrospinal fluid from t...
Medical Devices·79 affected·Dec 23, 2013
High RiskFDA
Aesculap, Inc.
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
Medical Devices·30 affected·Sep 20, 2013
High RiskFDA
Aesculap, Inc.
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Medical Devices·24 affected·Sep 19, 2013
High RiskFDA
Aesculap, Inc.
Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electr...
Medical Devices·85 affected·Sep 10, 2013
High RiskFDA
Aesculap, Inc.
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
Surgical Devices·217 affected·Jul 16, 2013
High RiskFDA
Aesculap, Inc.
ProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral body replacement or intervertebral body fusion to a...
Medical Implants·9 affected·Jun 18, 2013
High RiskFDA
Aesculap, Inc.
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Surgical Devices·59 affected·Jan 18, 2013
High RiskFDA
Aesculap, Inc.
Aesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal Catheter and FT075P 0 Ventric Cathet, w/Stylet and RT-ANG Gui...
Surgical Devices·11 affected·Jun 4, 2012