235 results
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19ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Clinical Chemistry Uric Acid; LN 7D76-20
FDA Recall
Terminated
·Abbott Laboratories Diagnostic Div·Product code CDO·March 18, 2004
Irrigation Clip 30; Intended to position and hold irrigation tubing during surgical procedures.
FDA Recall
Terminated
·The Anspach Effort, Inc.·Product code GDO·November 2, 2015
LIGACLIP Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex Trays), 10mm M/L Product Usage: The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a sterile, single patient use instrument designed to provide a means of ligation through ENDOPATH surgical trocars. The instrument delivers 20 titanium clips that individually advance after each firing. The shaft is made of a low glare material that minimizes reflective distortion. It is designed to rotate 360 in either direction. The rotating knob is located to allow for a one-handed technique.
FDA Recall
Terminated
·Ethicon Endo-Surgery Inc·Product code GDO·April 12, 2013
Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A Teleflex Company, Manufactured for: Weck Closure Systems, 2917 Weck Drive, Research Triangle park, NC 27709, USA.
FDA Recall
Terminated
·Product code GDO·May 21, 2003
LIGACLIP Endoscopic Rotating Multiple Clip Applier (ER320), 10mm M/L, bulk non-sterile Product Usage: The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a single patient use instrument designed to provide a means of ligation through ENDOPATH surgical trocars. The instrument delivers 20 titanium clips that individually advance after each firing. The shaft is made of a low glare material that minimizes reflective distortion. It is designed to rotate 360 in either direction. The rotating knob is located to allow for a one-handed technique.
FDA Recall
Terminated
·Ethicon Endo-Surgery Inc·Product code GDO·April 12, 2013
TEVADAPTOR Closed Drug Reconstitution and Transfer System, a closed system used to prepare drugs, including cytotoxic drugs, for intravenous infusion or injection. Model number is MG412110. The device is a single use device.
FDA Recall
Terminated
·Migada Inc.
P.O Box 888
Kiryat Shmona Israel·Product code LHI·December 18, 2008
Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code CBK·June 14, 2021
A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minimum Ventilatory Support, Facility Use
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code MNS·June 14, 2021
A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code MNS·June 14, 2021
Mito Red Light, Super Mobile
FDA Recall
Open, Classified
·MITO RED LIGHT INC·Product code ILY·February 12, 2025
Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
FDA Recall
Open, Classified
·Boston Scientific Neuromodulation Corporation·Product code LGW·April 29, 2026
MobileDiagnost wDR motorized portable diagnostic X-ray systems.
FDA Recall
Terminated
·Sedecal S.A. C/Pelaya, 9-13 Pol. Industrial Rio De Janiero Algete Spain·Product code IZL·August 6, 2014
Healing Abutment Conical Connection RP 0 3.6 x 5mm, REF: 36644, UDI: 07332747034462 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore chewing function. The Healing Abutment is intended to be used as a temporary component to an endosseous implant to allow healing of the soft tissue.
FDA Recall
Terminated
·Nobel Biocare Usa Llc·Product code DZE·May 28, 2019
Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1
FDA Recall
Open, Classified
·Busse Hospital Disposables, Inc.·Product code OGJ·October 21, 2022
Cirq Arm System 2.0
FDA Recall
Open, Classified
·Brainlab AG Olof-palme-str. 9 Munich Germany·Product code OLO·March 2, 2023
Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1
FDA Recall
Open, Classified
·Busse Hospital Disposables, Inc.·Product code OGJ·October 21, 2022
Brand Name: Paradise Ultrasound Renal Denervation System Product Name: Paradise Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
FDA Recall
Open, Classified
·ReCor Medical Inc.·Product code QYI·January 29, 2026
FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code QZI·June 25, 2025
LYSO Disk(TM) labeled as containing Actinomyces odontolyticus. Each LYSO Disk" unit contains six lyophilized pellets of a single microorganism strain, in a glass vial. Each vial is sealed and contains a desiccant to prevent adverse moisture accumulation. A LYFO Disk" catalog number ends in L.
FDA Recall
Terminated
·Microbiologics Inc·Product code JTR·March 2, 2017
Brand Name: Paradise Ultrasound Renal Denervation System Product Name: Paradise Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
FDA Recall
Open, Classified
·ReCor Medical Inc.·Product code QYI·January 29, 2026