335 results
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Sources: EU EUDAMED, US FDA
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Bair Hugger Temperature Management Blanket, Model 555 Pediatric Full Access Blanket. Use only with a Bair Hugger temperature managemen unit. Not Sterile. Do not use if primary packaging has been previously opened or is damaged. Arizant Healthcare Inc., 10393 West 70th Street, Eden Prairie, MN 55344 USA.
FDA Recall
Terminated
·Arizant Inc·Product code DWJ·March 11, 2005
FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend Stair Chair Powertraxx (Item #0731403/UDI-DI 00190790004064) not included in this action).
FDA Recall
Open, Classified
·Ferno-Washington Inc·Product code FPO·October 7, 2022
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the vena cava in the following situations: - Pulmonary thromboembolism when anticoagulants are contraindicated, - Failure of anticoagulant therapy for thromboembolitic disease, - Emergency treatment following massive pulmonary embolism where anticipate benefits of conventional therapy are reduce, and - Chronic, recurrent pulmonary embolism where anticoagulant therapy has failed, or is contraindicated.
FDA Recall
Terminated
·Cordis Corporation·Product code DTK·September 27, 2013
Medtronic (TiMesh), Screwdriver, 1.5mm, Cruciate, Self Tapping Shaft, Catalog Number 8001215 The 8001215 Screwdriver is a stainless steel part designed for use with cruciate-style screws in the firm''s TiMesh System. The product is sold in non-sterile, single unit packages. They are re-usable, and autoclavable.
FDA Recall
Terminated
·Medtronic Neurosurgery·Product code GXL·March 8, 2006
Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary thromboembolism when anticoagulants are contraindicated " Failure of anticoagulant therapy in thromboembolic disease " Emergency treatment following massive pulmonary embolism where anticipated benefits of conventional therapy are reduced " Chronic, recurrent pulmonary embolism where anticoagulant therapy has failed or is contraindicated
FDA Recall
Open, Classified
·Argon Medical Devices, Inc·Product code DTK·September 12, 2025
Plum 360 Infusion System, List number 30010.
FDA Recall
Terminated
·ICU Medical Inc·Product code FRN·October 30, 2017
Seimens Mevatron M-2 6700 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number 9401407, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Seimens Mevatron KD-2 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number: 9822685, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Seimens Mevatron M-2 6300 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number: 9401316, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron K-2 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number: 1940753, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron MDX-2 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model number 9401746, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron KDS-2 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number 9822693 and 9411588, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron M-2 6740 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position)Model Number: 9401506, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron KD2 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number:08515520, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron MD2 Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number: 09401654, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron M-2 PRIMUS mid-energy Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number :1940035, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
Siemens Mevatron M-2 PRIMUS hi-energy Medical Charged-Particle Radiation Therapy System; (Interlock #51 Jaw Field Position) Model Number 4504200, Siemens Medical Solutions, Concord, CA 94520
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·August 7, 2007
CADD Solis HSPCA Pump
FDA Recall
Open, Classified
·Smiths Medical ASD, Inc.·Product code MEA·April 10, 2025
MED-810A Zemits NDPrime Laser products
FDA Recall
Open, Classified
·Advance-Esthetic LLC·Product code GEX·October 9, 2023
Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
FDA Recall
Terminated
·Life Force of Tampa, LLC·Product code LGM·June 27, 2014