Aesculap, Inc.: 26 recalls on record

Recalls filed with 1 agency: FDA (26).

First recall on record: October 24, 2012. Most recent: June 19, 2024.

Risk classification: Class II: 25 · Class III: 1

Most recent recalls

DateAgencyProduct
June 19, 2024FDAAeos Robotic Digital Microscope, Product Code: PV010Z-2139-2024
March 13, 2024FDADISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures.Z-1247-2024
March 13, 2024FDADISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic proce…Z-1243-2024
March 13, 2024FDADISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.Z-1244-2024
March 13, 2024FDADISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic proced…Z-1245-2024
March 13, 2024FDADISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic proced…Z-1246-2024
February 7, 2024FDAMB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HO…Z-0867-2024
February 7, 2024FDAMB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBS…Z-0866-2024
March 9, 2016FDAColumbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revisio…Z-1043-2016
December 30, 2015FDAFlexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG Th…Z-0422-2016
August 12, 2015FDAS4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clam…Z-2326-2015
February 4, 2015FDAMiethke Shunt System accessories Product Usage: - The Miethke Shunt System is intend…Z-1012-2015
December 24, 2014FDAAesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shu…Z-0814-2015
December 10, 2014FDAThe Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum,…Z-0502-2015
July 16, 2014FDADafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Sur…Z-2024-2014
June 11, 2014FDAAesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System T…Z-1676-2014
February 26, 2014FDAAesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt syste…Z-0989-2014
January 15, 2014FDAAesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN¿ and mic…Z-0623-2014
December 25, 2013FDAAesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7Z-0492-2014
December 18, 2013FDAAesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator i…Z-0479-2014
November 27, 2013FDAAesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)Z-0361-2014
October 30, 2013FDAUNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments duri…Z-0031-2014
July 31, 2013FDAProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral bod…Z-1806-2013
March 6, 2013FDAAesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and…Z-0887-2013
February 20, 2013FDAAesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal Catheter and …Z-0805-2013

Questions about this company

How many recalls does Aesculap, Inc. have?
Recalert has 26 U.S. recalls on record for Aesculap, Inc., published between October 24, 2012 and June 19, 2024.
What was the most recent Aesculap, Inc. recall?
FDA recall Z-2139-2024, published June 19, 2024: Aeos Robotic Digital Microscope, Product Code: PV010
Which agencies have handled Aesculap, Inc. recalls?
Aesculap, Inc. appears as the recalling firm in recalls from: FDA (26).

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