Abbott Diabetes Care Inc. Class l

Company: Abbott Diabetes Care, Inc..
Date of Enforcement Report: 6/7/05
Class:I

PRODUCT
Abbott Diabetes Care, Inc. Blood Glucose Meters

REASON
The recalled Abbott blood glucose meters can inadvertently switch the glucose readings from mg/dL, the U.S. standard to mmol/L, the foreign standard. The unit of measure could change in the course of setting the time and date for the meters, when they are dropped or upon battery replacement. In the U.S., if the consumer does not realize that the units of measure changed from the U.S. standard to the foreign standard, misinterpretation of the test results could occur, potentially leading to hyperglycemia. Hyperglycemia is particularly harmful in pregnant women that could lead to fetal damage (abnormal fetal growth and altered organ development and maturation, fetal hypoxemia, spontaneous abortion, and congenital anomalies).

RECALLING FIRM/MANUFACTURER
Recalling Firm: Abbott Diabetes Care, Inc.,1360 S Loop Road,Alameda, CA 94502-7000.

Manufacturer: Abbott Diabetes Care, Inc.

About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

Upcoming Public Courses

IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software training course in Boise, Idaho. 3-Day course.

October 13-15, 2026

Limited Early Bird Registration: $995 / person
Non refundable but transferable.

Or just email training@softwarecpr.com for more info.

Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.