Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The Recalled by Abbott Diabetes Care, Inc. Due to Due to a manufacturing process issue that may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Abbott Diabetes Care, Inc. directly.
Affected Products
FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Quantity: 1,060,723 sensors
Why Was This Recalled?
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Where Was This Sold?
This product was distributed to 36 states: AL, AK, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NJ, NY, NC, OH, OK, PA, SC, SD, TX, UT, VA, WV, WI, WY
About Abbott Diabetes Care, Inc.
Abbott Diabetes Care, Inc. has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report