Lifescan Inc LifeScan OneTouch Ultra Primary Care Physician Demo Kits, Blood Glucose Meter Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LifeScan OneTouch Ultra Primary Care Physician Demo Kits, Blood Glucose Meter
Brand
Lifescan Inc
Lot Codes / Batch Numbers
Listing Number B026094, Code 90273 Kaban, all demo kits shipped between 04/08/2005 and 08/23/2005
Products Sold
Listing Number B026094, Code 90273 Kaban, all demo kits shipped between 04/08/2005 and 08/23/2005
Lifescan Inc is recalling LifeScan OneTouch Ultra Primary Care Physician Demo Kits, Blood Glucose Meter due to Users may inadvertently change units of measurement on demonstration kits of the OneTouch Ultra Blood Glucose Meters. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Users may inadvertently change units of measurement on demonstration kits of the OneTouch Ultra Blood Glucose Meters
Recommended Action
Per FDA guidance
A notification letter dated October 10, 2005 was issued to all health care professionals that requested the demo kit.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026