Every recall we track for Abbott Diabetes Care, Inc. — 13 in all — plus the complaints and injury reports the public filed about them.
Abbott Diabetes Care recalls FreeStyle Libre 3 Plus sensors with specific serial numbers due to potential carbon buildup causing incorrect low glucose readings. Affected units may need replacement to ensure accurate blood glucose monitoring.
Abbott Diabetes Care recalls FreeStyle Libre 3 Plus sensors with specific serial numbers due to potential carbon buildup causing incorrect low glucose readings. Affected units may need replacement to ensure accurate blood sugar monitoring.
Abbott Diabetes Care recalls FreeStyle Libre 3 Plus sensors with specific serial numbers due to potential carbon buildup causing incorrect low glucose readings. Affected units may need replacement.
Abbott Diabetes Care recalls FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code 00357599818005 due to manufacturing issues that may cause carbon buildup in the sensor, potentially leading to incorrect low glucose readings. Affected units have specific serial numbers and expiry dates.
Abbott recalls FreeStyle Libre 3 Sensors with serial numbers starting with T60001948 and 0FP5Z... that may show falsely high glucose levels, leading to incorrect insulin doses and missed hypoglycemia detection. Users should stop using affected sensors immediately.
Abbott recalls FreeStyle Libre 2 Readers (REF: 71951-01 and 71953-01) that may show "Incompatible Sensor" message if old sensor not used for full 14 days, causing delayed glucose results.
Abbott recalls FreeStyle Libre Reader models with lithium-ion batteries that may swell, overheat, or cause fire. Only use included charger. Stop using if damaged, swollen, or overheating.
Abbott Diabetes Care recalls FreeStyle Libre Reader models 71936-01, 71937-01, and 71938-01 due to lithium-ion battery swelling, overheating, or fire hazard. Only use included charger.
Abbott Diabetes Care recalls FreeStyle Libre Reader models 71951-01, 71952-01, and 71953-01 due to lithium-ion battery swelling, overheating, or fire hazard. Only use included charger; do not use damaged or swollen units.
Abbott recalls FreeStyle Libre 3 app for Android 13 OS versions 3.4.0 and below due to potential signal loss causing undetected glucose levels. Users may need to update or switch OS.
Abbott recalls FreeStyle Precision H blood glucose and ketone meters due to unapproved disinfection instructions that could cause infections if not handled properly.
Abbott recalls Optium EZ glucose meters due to unapproved disinfection instructions that could cause infections if not handled properly. Affected units lack FDA clearance for multiple-patient use.
Abbott Diabetes Care recalls Precision Xtra blood glucose and ketone meters with specific UDI numbers due to unapproved disinfection instructions that could cause infections if not handled properly.
