846 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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FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685
FDA Recall
Open, Classified
·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023
TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
FDA Recall
Open, Classified
·Full Vision Inc·Product code IOL·May 12, 2023
TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE
FDA Recall
Open, Classified
·Full Vision Inc·Product code IOL·May 12, 2023
Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps UPN/Catalog Number: MOO513330 The Radial Jaw 4 Large Capacity Inner Pouch, 240cm UPN M00513330 is a single unit which is packaged into a Box of 20 units (UPN M00513331), and a Box of 80 units (UPN M00513334). Single packaged units of M00513330 are not sold individually.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code FCL·May 6, 2010
Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps Box 80, 240cm UPN/Catalog Number: M00513334
FDA Recall
Terminated
·Boston Scientific Corporation·Product code FCL·May 6, 2010
TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929
FDA Recall
Open, Classified
·Full Vision Inc·Product code IOL·May 12, 2023
Portable Oxygen Analyzer
FDA Recall
Terminated
·Teledyne Analytical Instruments·Product code CCL·October 27, 2003
Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the AlterG Anti-Gravity Treadmill for rehabilitation.
FDA Recall
Terminated
·AlterG, Incorporated·Product code IOL·January 28, 2014
GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field Replaceable Unit P/Ns 408930-001 Rev E, 408930-002 Rev C. UPDATE: 3-30-2015: T2100 & T2000 Treadmills with power cord part numbers 408930-001, 408930-002, or 2028038-008 Also Field Replaceable Unit P/Ns 408930-001, 408930-002 Product Usage: Used for Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.
FDA Recall
Terminated
·GE Healthcare·Product code IOL·February 16, 2015
D-fend, (p/n 876446-HEL), and D-fend+ (p/n 881319-HEL) water trap. Used with Compact Airway Modules E/M-C(Ai)O(V)(X) and Cardiocap/5 monitors. Product Usage: Water traps are intended to protect the GE monitor from humidity, secretions and bacterial contamination when monitoring respiratory parameters. D-fend and D-fend+ water traps are used with Compact gas module E-C(Ai)O(V)(X) and CardioCap/5 monitors. The Datex-Ohmeda S/5 Compact Airway Module, E-CAiOVX family is indicated for monitoring hospital patients respiration (CO2, O2, N2O, anesthetic agents, anesthetic agent identification and respiration rate) ventilation (airway pressure, volume and flow) and gas exchange status (Oxygen Consumption VO2, Carbon Dioxide production VCO2, Respiratory Quotient RQ, and Energy Expenditure, EE). Gas exchange status monitoring is not indicated in the presence of N2O+O2 mixtures. The device is indicated for use by qualified medical personnel only.
FDA Recall
Terminated
·GE Healthcare·Product code CCL·April 24, 2015
Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps Inner Pouch 240cm, Box 20 UPN/Catalog Number: M00513331
FDA Recall
Terminated
·Boston Scientific Corporation·Product code FCL·May 6, 2010
GE Healthcare, Treadmill T2100. For Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.
FDA Recall
Terminated
·GE Healthcare·Product code IOL·March 12, 2015
FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928
FDA Recall
Open, Classified
·Full Vision Inc·Product code IOL·August 31, 2022
REF 20130-01 Spinning Spiros Closed Male Luer, Red Cap REF CH2000S-PC Spinning Spiros Closed Male Luer, Purple Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
FDA Recall
Open, Classified
·ICU Medical, Inc.·Product code N/A·March 16, 2021
Trifurcated Transpac IV Monitoring Kit w/Safeset Reservoir, 03 ml Squeeze Flush and 6 Needleless Valves, Item No. 011-46106-22 Transpac Trifurcated monitoring kit with Safeset Reservoir, squeeze flush and sampling ports. The monitoring kit is intended for measuring and montoring of fluid pressure, fluid infusion, and blood withdrawal.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code DRS·July 18, 2014
Hospira Intralock Lipid Compatible 3-Way Stopcock, Item Number 423830401 Indicated for fluid flow directional control and for providing access port(s) for administration of solutions.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code FMG·June 11, 2008
10" Smallbore Pentafuse Ext Set w/5 NanoClave", 5 Clamps, Rotating Luer, Part No. A1000, Item No. A1071 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administration of fluids to a patient through a cannula placed in the vein or artery.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code FPA·December 24, 2013
7" (18cm) Appx 0.32 ml, Smallbore Ext Set w/Remv MicroCLAVE Clear, NanoClave T-Connector, Clamp, Rotating Luer, Part No. A1000, Item No. A1009 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administration of fluids to a patient through a cannula placed in the vein or artery.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code FPA·December 24, 2013
7" (18 cm) Appx 0.24 ml, Smallbore Ext Set w/NanoClave", Clamp, Luer Lock, Part No. A1000, Item No. K7095-001 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administration of fluids to a patient through a cannula placed in the vein or artery.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code FPA·December 24, 2013
8" Smallbore Pentafuse Ext Set w/5 NanoClave", 5 Clamps, Rotating Luer, Part No. A1000, Item No. A1070 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administration of fluids to a patient through a cannula placed in the vein or artery.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code FPA·December 24, 2013