43 results
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22ms
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Sources: EU EUDAMED, US FDA
BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045150
FDA Recall
Open, Classified
·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023
BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045151
FDA Recall
Open, Classified
·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023
Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code LXH·May 23, 2024
Distractor Rack, REF 5598007, which may be packaged in Modular Distractor Set, Loaner Kit Number SPS03139; for use in spinal surgery
FDA Recall
Open, Classified
·Medtronic Sofamor Danek USA Inc·Product code LXH·November 19, 2021
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
FDA Recall
Open, Classified
·Intrinsic Therapeutics, Inc.·Product code LXH·July 25, 2024
TriALTIS TORQUE LIMITER, RATCHET, 11.3 Nm, Model Number 5161-00-5048 (G919509)
FDA Recall
Open, Classified
·Gauthier Biomedical, Inc.·Product code LXH·November 11, 2024
The Graft Tube is an optional instrument which, as designed, can be filled with flowable graft material, then advanced through the Access Portal. A Push Rod is then used to facilitate the manual deployment of the graft material out of the Graft Tube and adjacent to where the implant is to be placed, as supported within the Surgical Technique Guide.
FDA Recall
Open, Classified
·Spineology, Inc.·Product code LXH·September 16, 2024
Universal Chuck-The Universal Chuck is an Instrument Handle provided as an alternative instrument available for use in the TN-ADVANCED" Tibial Nailing System (TNA), TFN-ADVANCED" Proximal Femoral Nailing System (TFNA), RFN-ADVANCED" Retrograde Femoral Nailing System (RFNA), FRN-ADVANCED" Femoral Recon Nailing System (FRNA), and Flexible Monobloc Reamers. Instrument Handles are intended for holding instruments for manipulation during orthopedic surgery. Product No.: 03.043.001
FDA Recall
Open, Classified
·Synthes (USA) Products LLC·Product code LXH·December 22, 2021
Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
FDA Recall
Open, Classified
·Stryker GmbH Bohnackerweg 1 Selzach Switzerland·Product code LXH·March 28, 2025
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
FDA Recall
Open, Classified
·TriMed Inc.·Product code LXH·September 28, 2018
TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the labels is TriMed Inc., Santa Clarita, CA.
FDA Recall
Open, Classified
·TriMed Inc.·Product code LXH·September 28, 2018
EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
FDA Recall
Open, Classified
·Product code LXH·February 4, 2019
HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
FDA Recall
Open, Classified
·Mizuho OSI·Product code LXH·July 29, 2021
Exeter V40 Trial Head, 26mm, -3, Catalog Number 6364-8-026
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code LXH·May 3, 2023
Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
FDA Recall
Open, Classified
·Stryker GmbH Bohnackerweg 1 Selzach Switzerland·Product code LXH·March 28, 2025
COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
FDA Recall
Open, Classified
·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code LXH·February 24, 2025
Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Description: The Repeater Bone Tamp is a cylindrical shaft used to push bone graft material through a corresponding bone funnel into the FlareHawk interbody fusion device in spinal fusion procedures. Component: No
FDA Recall
Open, Classified
·Integrity Implants Inc.·Product code LXH·December 20, 2024
K-Wire, 1.35 mm x 170 mm
FDA Recall
Open, Classified
·Arthrex, Inc.·Product code LXH·March 25, 2022
COR Disposable Kit, 8 mm. Cartilage Transplant System.
FDA Recall
Open, Classified
·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code LXH·February 24, 2025
Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156
FDA Recall
Open, Classified
·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023