22 results
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50ms
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Sources: EU EUDAMED, US FDA
Fischer Medical Supply
FDA registration
Fischer Medical Supply·1 product·🇺🇸 United States
60 ML BD SYRINGE WITH BD LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·July 28, 2017
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·March 12, 2018
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and Paykel; Healthcare CosyCot and Kit Replacement Head Case Assembly It is designed to assist with the thermoregulation of infants weighing up to 10kg and is used by labor and delivery rooms and pediatric intensive care units. Infant Warmers Model Number (REF) IW910XXX, IW920XXX, IW931XXX, IW932XXX, IW933XXX, IW934XXX, IW951XXX, IW952XXX, IW953XXX, IW954XXX, IW980XXX, IW990XXX Spare Parts Model Number (REF) 043041129, 043041130, 043041131, 043042359, 648040142
FDA Recall
Terminated
·Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand·Product code FMT·November 6, 2014
Fisher & Paykel Healthcare reusable breathing circuit. Non-heated breathing circuit, 1.8m or 6 feet in length. Oxygen therapy delivery system for adult patient.
FDA Recall
Terminated
·Fisher & Paykel Healthcare, Ltd.·Product code BZO·November 19, 2012
remel RapID Yeast Plus System, 20 tests, Ref: R8311007, IVD, containing a 15-ml bottle of RapID Yeast Plus Reagent A and a 10-ml bottle of RapID Yeast Plus Reagent B. Product Usage: For the biochemical identification of medically important yeast and yeast-like organisms.
FDA Recall
Terminated
·Remel Inc·Product code JXB·April 4, 2013
Centurion Healthcare Products Pump Fill Kit DT10175. CONTENTS: 1 CSR WRAP, 2 GLOVES, 1 FENESTRATED DRAPE, 1 EXTENSION LINE Approx. Priming Vol.: 0.3mL, 1 SYRINGE, 1 Exel Huber NEEDLE, 1 ChloraPrep(R), 1 TRAY The recalled Exel Huber Needles are used to access subcutaneously implanted ports used for the withdrawal of blood samples and infusion of medication. The firm places the recalled needles in pump fill kit.
FDA Recall
Terminated
·Centurion Medical Products·Product code FMI·February 1, 2010
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829570, UDI: (01) 00801741027192 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code LJT·March 25, 2021
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829500, UDI: (01) 00801741027185 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code LJT·March 25, 2021
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 5829502, UDI: (01)00801741027406 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code LJT·March 25, 2021
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Importer
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