Aesculap, Inc.
29 recalls on record · Latest: Nov 5, 2025
FDA Devices Moderate Nov 5, 2025
Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Product Descriptio…
FDA Devices Moderate Nov 5, 2025
Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A Product Description: REDU…
FDA Devices Moderate Mar 19, 2025
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-…
FDA Devices Moderate Mar 19, 2025
Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Fo…
FDA Devices Moderate Mar 19, 2025
Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2) REF BH104R, Hartmann Mosquito FCSDEL STR 100MM; …
FDA Devices Moderate Jun 19, 2024
Aeos Robotic Digital Microscope, Product Code: PV010
FDA Devices Moderate Mar 13, 2024
DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
FDA Devices Moderate Mar 13, 2024
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.
FDA Devices Moderate Mar 13, 2024
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.
FDA Devices Moderate Feb 7, 2024
MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"
FDA Devices Moderate Feb 7, 2024
MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";
FDA Devices Moderate Mar 9, 2016
Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use i…
FDA Devices Moderate Dec 30, 2015
Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the implantation…
FDA Devices Moderate Dec 30, 2015
Flexible Drill; SJ723R; NON STERILE; B Braun Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A…
FDA Devices Moderate Dec 30, 2015
Tray Set containing multiple instruments and may contain the flexible bone awl, flexible drill and/or flexible screw driver in varying amounts depend…
FDA Devices Moderate Aug 12, 2015
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 tightening the …
FDA Devices Moderate Feb 4, 2015
Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles o…
FDA Devices Low Dec 24, 2014
Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of …
FDA Devices Moderate Dec 10, 2014
The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.
FDA Devices Moderate Jul 16, 2014
Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Surgical Suture, additional label affixed on the box states the…
FDA Devices Moderate Jun 11, 2014
Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is intended to shut cerebrospinal fl…
FDA Devices Moderate Feb 26, 2014
Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut cerebrospinal fluid from the lateral v…
FDA Devices Moderate Dec 25, 2013
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
FDA Devices Moderate Dec 18, 2013
Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power f…
FDA Devices Moderate Nov 27, 2013
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
FDA Devices Moderate Oct 30, 2013
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
FDA Devices Moderate Jul 31, 2013
ProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral body replacement or intervertebral body fusion to aid in the su…
FDA Devices Moderate Mar 6, 2013
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
FDA Devices Moderate Feb 20, 2013