547 results
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12ms
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Sources: EU EUDAMED, US FDA
Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Column Distal Radius Plate - 6 Head, 10 Shaft, Standard Left - 139mm
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·December 19, 2025
Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Column Distal Radius Plate - 6 Head, 14 Shaft, Standard Left - 186mm Component: No
FDA Recall
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·Tyber Medical·Product code HRS·December 19, 2025
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
FDA Recall
Open, Classified
·Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom·Product code LDD·May 8, 2023
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
FDA Recall
Open, Classified
·Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom·Product code LDD·May 9, 2024
Portable X-ray system
FDA Recall
Open, Classified
·DIGIMED CO., LTD
401, 402, 406~411-ho, A-dong 101, Gasan digital 2-ro, Geumcheon-Gu
Seoul Korea (the Republic of)·Product code EHD·June 19, 2025
Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
FDA Recall
Open, Classified
·Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom·Product code LDD·October 28, 2024
STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15 Defibrillation is indicated for the termination of certain potentially fatal arrhythmias, such as ventricular fibrillation and symptomatic ventricular tachycardia. Synchronized cardioversion is indicated for the treatment of atrial fibrillation, atrial flutter, paroxysmal supraventricular tachycardia, supraventricular tachycardia, and in relatively stable patients, ventricular tachycardia.
FDA Recall
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·Physio-Control, Inc.·Product code LDD·August 9, 2024
ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnosis and treatment of gentamicin overdose and in monitoring levels of gentamicin to help ensure appropriate therapy.
FDA Recall
Open, Classified
·Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany·Product code LCD·April 24, 2020
STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use by a health care provider to sterilize medical products by means of pressurized steam. Model: G4 621103
FDA Recall
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·Scican Ltd.·Product code FLE·June 22, 2023
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
FDA Recall
Open, Classified
·NOXBOX LTD·Product code MRN·September 9, 2025
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
FDA Recall
Open, Classified
·NOXBOX LTD·Product code MRN·September 9, 2025
NOxBOXi Nitric Oxide Delivery System
FDA Recall
Open, Classified
·NOXBOX LTD·Product code MRN·July 19, 2023
STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use by a health care provider to sterilize medical products by means of pressurized steam. Model: G4 622303
FDA Recall
Open, Classified
·Scican Ltd.·Product code FLE·June 22, 2023
Medicina Oral Tip Syringe 2.5ml Code: OT25
FDA Recall
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·Medicina Uk Ltd·Product code KYW·July 4, 2022
Constellation Procedure Pak
FDA Recall
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·Alcon Research, LTD.·Product code HQC·June 28, 2023
Centurion FMS Pak
FDA Recall
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·Alcon Research, LTD.·Product code HQC·June 28, 2023
Alcon Custom Pak
FDA Recall
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·Alcon Research, LTD.·Product code HQC·June 28, 2023
Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022
Legion FMS Pak
FDA Recall
Open, Classified
·Alcon Research, LTD.·Product code HQC·June 28, 2023
Medicina Reusable Oral syringe 5ml Code: OTH05
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022