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 System
Lithium-ion batteries in glucose monitoring system readers may swell, overheat, or pose fire hazard. Only use the charging cable/power adapter included with readers. Do not use reader if it is damaged, cracked,…
Read the official notice →- Date
- 2023-04-12
- Country
- United States
- Brand
- Abbott Diabetes Care
- Product
- FreeStyle Libre Reader, REF: 71951-01, 71952-01, 71953-01 a component of the FreeStyle Libre 2 Flash Glucose Monitoring System
- Classification
- Class I
- Units
- U.S. Nationwide.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Abbott Diabetes Care recalls
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FDA · DeviceAbbott Diabetes Care, Inc.US Nationwide distribution in the states of NY, CA, NJ, UT, PA, MS, OH, TX,…Official notice → - 2023-08-23
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Abbott Diabetes Care, Inc. recalls FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
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FDA · DeviceAbbott Diabetes Care, Inc.US Nationwide distribution in the states of CA, FL, MI, NY, OH, TX, UT, VA.Official notice →
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