217 results
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Sources: EU EUDAMED, US FDA
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PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
FDA Recall
Open, Classified
·Nuvasive Specialized Orthopedics Inc·Product code HSB·February 12, 2021
PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
FDA Recall
Open, Classified
·Nuvasive Specialized Orthopedics Inc·Product code HSB·February 12, 2021
Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
FDA Recall
Open, Classified
·Nuvasive Specialized Orthopedics Inc·Product code HSB·February 12, 2021
07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
FDA Recall
Terminated
·Vascular Technology, Inc.·Product code DPW·May 28, 2014
Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and fractures of the proximal tibia and distal femur.
FDA Recall
Terminated
·Arthrex, Inc.·Product code HRS·March 11, 2021
Zimmer Natural Nail Tibial Nail - Yellow 8.3mm, Model Number 47249534008 Product Usage - The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone. Indications for the Tibial nails include the following in the tibia: Compound and simple shaft fractures Proximal, metaphyseal and distal shaft fractures Segmental fractures Comminuted fractures Fractures involving osteopenic and osteoporotic bone Pathological fractures Fractures with bone loss Pseudoarthrosis, non-union, mal-union and delayed union Periprosthetic fractures Surgically created defects such as osteotomies. Product Usage - The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone. Indications for the Tibial nails include the following in the tibia: Compound and simple shaft fractures Proximal, metaphyseal and distal shaft fractures Segmental fractures Comminuted fractures Fractures involving osteopenic and osteoporotic bone Pathological fractures Fractures with bone loss Pseudoarthrosis, non-union, mal-union and delayed union Periprosthetic fractures Surgically created defects such as osteotomies.
FDA Recall
Terminated
·Zimmer Biomet, Inc.·Product code HSB·July 30, 2018
.045 X 6 ST Guide Wire, Part number 45-0029-S, Sterile 10 pack of WS-1106ST and has a 6 inch length and 0.045 inch diameter. .054 X 7 ST Guide Wire, Part number 45-0031-S, Sterile 10 Pack of WS-1407ST and has a 7 inch length and 0.054 inch diameter. These guide wires are an orthopedic manual surgical instrument.
FDA Recall
Terminated
·Acumed LLC·Product code LXH·February 17, 2017
Crosslock DVR ePAK -Sterile, Ref 81180050, are complete surgical sets including plates, screws, and instruments for orthopedic fixation The Cross lock DVR ePAK Volar Rim Plates system is intended for fixation of fractures, mal unions, and osteotomies involving the distal radius. The DVR Wrist ePAK system is intended stabilization and fixation of small bone fragments in fresh fractures, revision procedures, joint fusion and reconstructions of small bones of the hand, foot, radius, ulna, ankle, humerus, scapula and pelvis, particularly in osteopenic bone.
FDA Recall
Terminated
·Biomet, Inc.·Product code LXT·January 29, 2016
NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL GSP30-SWE-INTL GSP30-ENG-INT GSP30-MAL-INTL GSP30-SPA-INT NasoGel Spray is a saline-based gel formula that can be sprayed to moisturize and lubricate dry and irritated anterior or front of nasal passages caused by dry climate and indoor heat.
FDA Recall
Open, Classified
·Neilmed Pharmaceuticals Inc·Product code KCJ·December 28, 2024
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
FDA Recall
Completed
·Acumed LLC·Product code HWC·March 9, 2022
4.0mm x 12mm Cannulated Screw, Short Thread; Part number 3005-40012
FDA Recall
Completed
·Acumed LLC·Product code HWC·March 9, 2022
Hemashield Gold Woven and Knitted Double Vascular Grafts.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·May 24, 2010
AlboGraft Woven with Collagen, Straight 15x26 Catalog Number: ATC1526 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Recall
Terminated
·LeMaitre Vascular, Inc.·Product code MAL·June 17, 2013
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·April 7, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch, Product Code: M00202175834P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·April 7, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175732P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·April 7, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175426T0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·April 7, 2020
Hemashield Platinum Woven Double Velour TAAA Vascular Grafts.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·May 24, 2010
AlboGraft Knitted with Collagen, Straight 60x07 Catalog Number: AMC6007 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Recall
Terminated
·LeMaitre Vascular, Inc.·Product code MAL·June 17, 2013
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175914P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MAL·April 7, 2020