10,000 results
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92ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIFESCAN INC.
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code CFR·August 7, 1997
ONE TOUCH ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN SCOTLAND LTD.·Product code CGA·February 27, 2024
ONE TOUCH ULTRA TEST STRIPS
FDA Adverse Event
Death
·LIFESCAN, INC.·Product code NBW·January 31, 2007
ONE TOUCH ULTRA TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·August 12, 2023
OT ULTRA TEST STRIPS
FDA Adverse Event
Malfunction
·UNKNOWN·Product code CGA·August 12, 2023
OT ULTRA TEST STRIPS
FDA Adverse Event
Malfunction
·UNKNOWN·Product code CGA·August 12, 2023
ONE TOUCH HORIZON TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·August 12, 2023
METER C - OT II
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code CFR·February 4, 2002
SYSTEM TEST, BLOOD GLUCOSE, OVER THE COUNTER
FDA Adverse Event
Malfunction
·UNKNOWN·Product code NBW·August 12, 2023
ONE TOUCH ULTRA TEST STRIPS #100
FDA Adverse Event
Injury
·LIFESCAN, INC·Product code NBW·July 23, 2008
LifeScan brand OneTouch Ultra Test Strip used in LifeScan Blood Glucose Meter; Part Number 020-244-07; Distributed and Manufactured by: LifeScan, Inc., 1000 Gibraltar Drive, Milpitas, CA 95037
FDA Recall
Terminated
·Lifescan Inc·Product code CGA·November 17, 2003
ONE TOUCH ULTRA
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code CFR·May 30, 2001
Lifescan OneTouch SureStep Meter Blood Glucose monitoring system,Product is distributed by LifeScan, Inc., 1000 Gibraltar Dr., Milpitas, CA 95037
FDA Recall
Terminated
·Lifescan Inc·Product code CGA·September 9, 2005
LifeScan brand OneTouch Ultra Meter - Owner''s Booklet; Product is manufactured and distributed by LifeScan, Inc., 1000 Gibraltar Dr., Milpitas, CA 95037
FDA Recall
Terminated
·Lifescan Inc·Product code NBW·November 21, 2003
LifeScan OneTouch Data Management Software Version 1.0, Part Number: 021-722-01(for OneTouch Select and UltraMini (Download) Blood Glucose Meters), LifeScan Inc, Milpitas, CA 95037.
FDA Recall
Terminated
·Lifescan Inc·Product code NBW·December 18, 2007
OneTouch SureStep and SureStep Pro Test strips, for use with the OneTouch SureStep Blood Glucose Meters, in 100 count and 50 count packaging distributed by LifeScan Inc., Milpitas, CA, Manufactured by LifeScan Puerto Rico Medical device for quantitative measurement of glucose in whole blood for use in home settings (SureStep).
FDA Recall
Terminated
·Lifescan Inc·Product code NBW·February 24, 2010
LifeScan brand OneTouch Sure Step- Blood Glucose Monitoring System Test Strips, 50 strips per package, Distributed and Manufactured by: LifeScan, Inc., 1000 Gibraltar Drive, Milpitas, CA 95037
FDA Recall
Terminated
·Lifescan Inc·Product code NBW·September 29, 2006
OneTouch SureStep Pro Test strips, for use with the OneTouch SureStep Pro Blood Glucose Meters, in 50 count packaging distributed by LifeScan Inc., Milpitas, CA, Manufactured by LifeScan Puerto Rico Medical device for quantitative measurement of glucose in whole blood for use in hospital and clinical settings. The product is also for use in quantitative measurement of glucose in venous, capillary, arterial and neonatal whole blood samples. This system can also be used by lay users at home.
FDA Recall
Terminated
·Lifescan Inc·Product code NBW·February 24, 2010
LifeScan brand One Touch -Sure Step Pro- Blood Glucose Monitoring System Test Strips, 50 strips per package, Distributed and Manufactured by: LifeScan, Inc., 1000 Gibraltar Drive, Milpitas, CA 95037
FDA Recall
Terminated
·Lifescan Inc·Product code CGA·September 29, 2006
OneTouch Verio IQ Blood Glucose Monitoring System Kit; One Touch Verio IQ Blood Glucose IQ Blood Glucose Monitoring Starter Kit; One Touch Verio IQ Blood Glucose Monitoring Warranty Kit. Distributed by : LifeScan, Inc. Milpitas, CA 95035 for: LifeScan Europe Division of Cilag GmBH International 6300 Zug Switzerland Meter made in China. Intended to be used for the quantitative measurement of glucose in fresh capillary whole blood.
FDA Recall
Terminated
·Lifescan Inc·Product code LFR·February 21, 2012