173 results
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28ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 42MM / XL25/ STER. Product Code: 04.045.342TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
FDA Recall
Open, Classified
·Synthes (USA) Products LLC·Product code JDS·September 26, 2025
LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
FDA Recall
Open, Classified
·Synthes (USA) Products LLC·Product code JDS·September 26, 2025
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
Newport s N-LHP-928(j) units if sold as a laser head/power supply set, and N5-LPL-944-080 and N6-LPL-944-080 if sold as a power supply alone.
FDA Recall
Open, Classified
·Product code RFN·March 27, 2024
p-Chip Wand Reader
FDA Recall
Open, Classified
·p-Chip Corporation·Product code RFN·March 3, 2021
Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm x 75cm (CFN CH05-40-75US), 6mm x 40mm x 75cm (CFN CH06-40-75US), 7mm x 40mm x 75cm (CFN CH07-40-75US), 8mm x 40mm x 75cm (CFN CH08-40-75US), 9mm x 40mm x 75cm (CFN CH09-40-75US), 10mm x 40mm x 75cm (CFN CH10-40-75US), 12mm x 40mm x 75cm (CFN CH12-40-75US)
FDA Recall
Open, Classified
·Product code LIT·September 19, 2024
Oxford/Oxbridge AFN End Cap 10 mm x 5 mm tp 12 mm x10 mm The end caps are a circular disk with a small threaded shaft to be screwed to the distal end of the Nail.
FDA Recall
Terminated
·Ortho Solutions Inc·Product code HSB·April 19, 2017
TourniKwik Tourniquet Set (CFN 79012)
FDA Recall
Open, Classified
·Medtronic Perfusion Systems·Product code GDJ·May 16, 2024
Enhanced Verify Evaluation Handset (CFN HH90130FA)
FDA Recall
Open, Classified
·Medtronic Neuromodulation·Product code EZW·April 3, 2025
Puritan Bennett 560 Ventilator, PB560, CFN 4096600
FDA Recall
Open, Classified
·Covidien Llc·Product code QOS·August 19, 2022
InPen App, Model/CFN Number: MMT-8061 (Android Users)
FDA Recall
Open, Classified
·Medtronic MiniMed, Inc.·Product code NDC·November 13, 2025
O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
FDA Recall
Terminated
·Medtronic Navigation, Inc.-Littleton·Product code OWB·November 15, 2019
Covidien Emprint Ablation Catheter with Thermosphere Technology Bronchoscopic Ablation, CFN CA108L1
FDA Recall
Terminated
·Covidien Llc·Product code NEY·September 29, 2021
InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users)
FDA Recall
Open, Classified
·Medtronic MiniMed, Inc.·Product code NDC·June 16, 2025
Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72
FDA Recall
Completed
·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVY·November 8, 2021
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); CFN: SIGSDL45CTVT;
FDA Recall
Open, Classified
·Product code GDW·September 25, 2025
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
FDA Recall
Open, Classified
·Medtronic Neuromodulation·Product code LGW·December 3, 2025
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
FDA Recall
Open, Classified
·Product code GDW·September 25, 2025
Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product Number/CFN: 178083, 178093, 178094
FDA Recall
Open, Classified
·Product code GEI·March 5, 2021
Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems. Product Number/CFN: 186-0208 UDI-Device Identifier (GTIN/UPN): 10884521130319
FDA Recall
Open, Classified
·Covidien LLC·Product code OLW·July 26, 2018