Aesculap Implant Systems LLC: 19 recalls on record

Recalls filed with 1 agency: FDA (19).

First recall on record: July 11, 2012. Most recent: September 7, 2022.

Risk classification: Class II: 19

Most recent recalls

DateAgencyProduct
September 7, 2022FDAAesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multis…Z-1638-2022
August 10, 2022FDAPRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product…Z-1482-2022
July 27, 2022FDAENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee…Z-1391-2022
July 27, 2022FDAMODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Se…Z-1410-2022
July 27, 2022FDAAESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code…Z-1444-2022
September 29, 2021FDAUnivation X System knee implant devices as follows: Catalog/Product: NL470 UNIVATION F…Z-2509-2021
March 25, 2020FDACOLUMBUS CRA/PSA TIB.PLAT.CEMENTED, Knee implant components, various sizes, model nos. N…Z-1480-2020
March 25, 2020FDACOLUMBUS CR/PS TIB.PLAT.PLASMAPORE, Knee implant components, various sizes, model nos. N…Z-1479-2020
March 25, 2020FDAColumbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN…Z-1478-2020
March 7, 2018FDAproSA Tool Set used to adjust and verify the proSA Adjustable Shunt System Shunt, cent…Z-0809-2018
February 21, 2018FDAELAN 4 Blade: ELAN 4 1-RING PIN CUTTER D1.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D1.5 ELAN …Z-0621-2018
February 21, 2018FDAThe ELAN 4 Air System is intended for high speed cutting, sawing and drilling of bone in …Z-0623-2018
May 24, 2017FDAGE426R; HI-LINE XS DIAMOND BURR X-CRS.I D4.5MM; GE426SU; HI-LINE XS DISP.DIAM.BURR X-C…Z-2089-2017
May 24, 2017FDAGP321R; ELAN 4 2-RING DIAMOND BURR COARSE D2.3; GP322R; ELAN 4 2-RING DIAMOND BURR COA…Z-2088-2017
April 19, 2017FDAAESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent T…Z-1814-2017
February 22, 2017FDAGN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessoriesZ-1218-2017
September 19, 2012FDAAesculap S4 Element 4.5mm Polyaxial Screws (ST240T, ST241T, ST242T, ST243T, ST244T, and S…Z-2333-2012
August 8, 2012FDAAesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD 9 degree Trial Implant…Z-2114-2012
July 11, 2012FDAS4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Revision Instruments…Z-1934-2012

Questions about this company

How many recalls does Aesculap Implant Systems LLC have?
Recalert has 19 U.S. recalls on record for Aesculap Implant Systems LLC, published between July 11, 2012 and September 7, 2022.
What was the most recent Aesculap Implant Systems LLC recall?
FDA recall Z-1638-2022, published September 7, 2022: Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar, thoracic and sacral spine. Article Number: 52758014
Which agencies have handled Aesculap Implant Systems LLC recalls?
Aesculap Implant Systems LLC appears as the recalling firm in recalls from: FDA (19).

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