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Web2 days ago · 04/12/23 5:00 PM PST. On April 6, 2024, the FDA issued a Class I Recall of Abbott’s FreeStyle Libre ®, FreeStyle Libre ® 14 day, and FreeStyle Libre ® 2 Readers in the United States. A medical device recall means a firm’s removal or correction of a medical device. In this case, Abbott is correcting the product labeling and not physically ... WebApr 14, 2024 · The FreeStyle Libre 3 system is the latest generation in Abbott's FreeStyle Libre portfolio – the most prescribed and affordable integrated continuous glucose monitoring (iCGM) system in the United States 1, 2; With a standalone reader, Abbott is working 3 to have the FreeStyle Libre 3 system available to Medicare beneficiaries who … eagle industries storage racks
FDA Clears Reader for Abbott
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