Devices

Device Recall OneTouch Ultra Test strip

Model / Serial
Part numbers 020-245-07 (100 pack), 020-244-07 (50 pack), 020-963-01 (50 pack mail order). Expiration dates 08/2007 through 11/2008.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide; USA, Europe, Middle East, Africa, Latin America and Canada.
Product Description
OneTouch Ultra Test strip, a component of the following OneTouch Ultra Glucose monitoring systems: a)OneTouch Ultra, b) OneTouch InDuo, c) OneTouch Ultra2, d) OneTouch UltraMini, e) OneTouch UltraSmart. 25 strips per vial. Product comes in packs of 100 and 50. (Part numbers: 020-245-07, 020-244-07, 020-963-01)
Manufacturer
Lifescan Inc
1 Event
- Recall of Device Recall OneTouch Ultra Test strip

Manufacturer

Lifescan Inc

Manufacturer Address
Lifescan Inc, 1000 Gibraltar Dr, Milpitas CA 95035-6312
Source
USFDA

One device with a similar name

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Device Recall OneTouch Ultra Test Strips

Model / Serial
Lot number 2528640, par tnumber 020-245-07, Expiration date April 2006
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
7 direct consignees (2 wholesale dealers and 5 distributors_ located in CA, PA, IL, WI, MN, SD, OK, CN, MA, MI.
Product Description
LifeScan OneTouch Ultra Test strips, lot number 2528640
Manufacturer
Lifescan Inc

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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