Certain Abbott Glucose Monitors Are Recalled

The FDA has reported that, based on medical device maker Abbott Laboratory’s company data, there have been 860 serious injuries connected to the recall of certain glucose monitoring sensors. Internal testing at the manufacturer determined that certain sensors can offer incorrect readings of low glucose. The consequences of this may involve injuries, complications, or even death. If you were harmed by one of the FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases around the nation with which we’ve been involved.

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In November 2025, Abbott issued a medical device correction, reporting that there had been 736 severe adverse events and deaths connected to certain affected glucose monitors. These events and deaths occurred on an international scale. When incorrect glucose readings go without detection, inappropriate treatment decisions for diabetic people may be made. For example, patients may consume excess carbohydrates or may skip or delay insulin doses.

Around 3 million Libre 3 and Libre 3 Plus sensors from a specific production line, around half of which were used or have expired were affected. The FDA issued an early alert in December. In January, the FDA classified it as a Class I recall, which is the most serious type of recall, on January 14, a company spokesperson told Reuters. Class I recalls occur when an affected product could cause serious injury or death if consumers continue to use it.

The affected products and models are as follows. The FreeStyle Libre 3 Sensor, Model Numbers 72081-01 and 72080-01, with unique device identifiers 00357599818005 and 00357599819002 are affected. Likewise, the FreeStyle Libre 3 Plus Sensor, Model Numbers: 78768-01 and 78769-01, with Unique Device Identifiers 00357599844011 and 00357599843014 are affected. The FreeStyle Libre 3 readers and mobile apps are not affected by this recall, and neither are other Libre products or Abbott biowearables.

The company has said that it has identified and resolved the reason for the issue. The problem relates to one of its production lines that manufactures the Libre 3 and Libre 3 Plus sensors.

You should figure out whether your sensor is an affected one by identifying the serial number on the label at the bottom of the sensor applicator or carton and checking www.FreeStyleCheck.comExternal Link Disclaimer. Abbott has offered to replace any sensor that may be affected without charge. If your sensor is affected, you should contact your doctor and discontinue using it.

What if you have already been injured by one of the affected sensors? You may be able to recover damages in a product liability lawsuit. These lawsuits can be pursued when a device is defective in terms of its manufacturing, design, or marketing. It is typically necessary to retain experts to review whether a product has defects and whether those defects caused the relevant injuries.

Consult an Experienced Product Liability Attorney

If you or a loved one was harmed by the Abbott glucose monitors that have been recalled, call the knowledgeable Chicago-based product liability lawyers of Moll Law Group to determine whether you have a viable basis to sue for damages.  If our firm can establish liability for a defective monitor, we may be able to recover economic and noneconomic damages on your behalf. We are committed to fighting for people around the country. Complete our online form or call us at 312.462.1700.