Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Connected Blood Glucose Meter Recalled by Telcare, LLC Due to Telcare, LLC has received customer complaints related to...
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 Telcare, LLC directly.
Affected Products
Philips Connected Blood Glucose Meter, BGM 4; Model Number: TM0009;
Quantity: 34,764 units
Why Was This Recalled?
Telcare, LLC has received customer complaints related to battery expansion/swelling for its Philips Connected Blood Glucose Meter (i.e., BGM 4 brand name) Monitoring System.. The issue was identified by post market surveillance data (customer complaints) - events of battery expansion/swelling and associated symptoms, e.g., leading to the device's removable back cover (battery port) to separate. If there is a loss of primary function of the device due to the described device defect, an immediate health consequence that may result is prolonged hypoglycemia or hyperglycemia due to delay in treatment, as the blood glucose measurement is not available to guide treatment. In a worst-case situation, there is potential for battery swelling to result in explosion of the battery and/ or device. Exposure to explosion, and subsequently projectiles from the explosion, may result in several immediate health consequences, including concussion, headache, dizziness, eye irritation, blurred vision, eye injury, and vision impairment.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Telcare, LLC
Telcare, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report