Reported Apr 24, 2013 · Terminated
All OneTouch Verio IQ Blood Glucose Meters sold as: Verio IQ System Kits - Meter; Verio IQ Starter kits - Meter; Verio…
Lifescan Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Lifescan Inc · 1000 Gibraltar Dr · Milpitas, CA · 95035-6301
Is this the product you have?
- All OneTouch
- Verio IQ Blood Glucose Meters sold asVerio IQ System Kits - Meter; Verio IQ Starter kits - Meter; Verio IQ Warranty Meter
- Product UsageThe OneTouch¿ Verio IQ Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips. The system is intended to be used by a single patient and should not be used for testing multiple patients. The OneTouch¿ Verio IQ Blood Glucose Monitoring System is intended for self-testing outside the body (in vitro diagnostic use) by people with diabetes at home as an aid to monitor the effectiveness of diabetes control
- Lot codes and dates
- Part numbersVerio
- IQ Systems Kits
022 267-01022 267-01022 267-03
- Verio IQ Starter Kits
022 268 01022 268-02
- Verio IQ Warranty Kits
022 275 01022 275 02. All lots and serial numbers
- Amount recalled
- US 710,413
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
The Verio IQ meter will shut off and revert to set up mode at glucose values above 1023 instead of displaying EXTREME HIGH GLUCOSE.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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