Abbott Diabetes Care, Inc. recalls
Every recall we track for Abbott Diabetes Care, Inc. — 13 in all, from 2019–2025 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Abbott Diabetes Care, Inc. more than tripled in 2025 (4, up from 1 in 2024). 8% rated “stop using now”.
All FDA recall records for Abbott Diabetes Care, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 3 | 0 | 0 | 3 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 5 | 0 | 0 | 5 |
| 2024 | 1 | 0 | 0 | 0 | 1 |
| 2025 | 0 | 1 | 3 | 0 | 4 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Abbott Diabetes Care, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Abbott Diabetes Care, Inc. recalls
6 shown- Use cautionMedical device
Abbott Diabetes Care, Inc. recalls FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the
Abbott Diabetes Care is recalling FreeStyle Libre 14 Day Sensors due to potential failure to measure glucose levels accurately. Check if your sensor serial number is affected.
FreeStyle LibreNov 24, 2025 - Stop using nowMedical device
Abbott Diabetes Care, Inc. recalls FreeStyle Libre 3 Sensors, REF: 72081-01, component of the FreeStyle Libre 3 Continuous Glucose Monitoring System
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.
AbbottJul 24, 2024 - Use cautionMedical device
Abbott Diabetes Care, Inc. recalls FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
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 Diabetes CareJul 12, 2023 - Use cautionMedical device
Abbott Diabetes Care, Inc. recalls FreeStyle Libre Reader, REF: 71951-01, 71952-01, 71953-01 a component of the FreeStyle Libre 2 Flash Glucose Monitoring
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 Diabetes CareFeb 13, 2023 - Use cautionMedical device
Abbott Diabetes Care, Inc. recalls FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System
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 Diabetes CareFeb 9, 2023 - Use cautionMedical device
Abbott Diabetes Care, Inc. recalls Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144
Abbott recalls Precision Xtra meters due to uncleared disinfection instructions that may cause infection. Check your device UDI and follow safety guidelines.
AbbottNov 14, 2019
Abbott Diabetes Care, Inc. recall questions
How many recalls has Abbott Diabetes Care, Inc. had?
13 recalls from Abbott Diabetes Care, Inc. are on record with U.S. safety agencies, from 2019–2025.
What is the most recent Abbott Diabetes Care, Inc. recall?
Abbott Diabetes Care, Inc. recalls FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the, dated Nov 24, 2025. Every Abbott Diabetes Care, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Abbott Diabetes Care, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Abbott Diabetes Care, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.