Reported Apr 12, 2023 · Ongoing

FreeStyle Libre Reader, REF: 71525-01, 71701-01, 71739-01 a component of the FreeStyle Libre Flash Glucose Monitoring…

Abbott Diabetes Care, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Abbott Diabetes Care, Inc. · 1360 S Loop Rd · Alameda, CA · 94502-7000

Is this the product you have?

  • FreeStyle Libre Reader
  • REF71525-01, 71701-01, 71739-01 a component of the FreeStyle Libre Flash Glucose Monitoring System
Lot codes and dates

3 of 3 products · 118 lot codes

Recalled lot codes, grouped by product number
REFUDI-DILot
71525-01357599000219
  • 02Y702D
  • 01Y699D
  • 02Y699D
  • 01Y698D
  • 02Y697D
  • 04Y690D
  • 03Y690D
  • 01Y683D
  • 02Y683D
  • 01Y674D
  • 02Y672D
  • 01Y669D
  • 02Y666D
  • 01Y659D
  • 02Y658D
  • 02Y656D
  • 04Y655D
  • 01Y655D
  • 01Y652D
  • 02Y653D
  • 03Y653D
  • 03Y651D
  • 01Y641D
  • 02Y638D
  • 01Y637D
  • 02Y635D
  • 01Y629D
  • 03Y628D
  • 01Y628D
  • 02Y628D
  • 02Y621D
  • 02Y622D
  • 02Y620D
  • 02Y608D
  • 04Y608D
  • 01Y608D
  • 01Y603D
  • 03Y599D
  • 04Y600D
  • 02Y596D
  • 06Y596D
  • 03Y596D
  • 07Y547D
  • 07Y546D
  • 08Y546D
  • 05Y540D
  • 06Y538D
  • 05Y537D
  • 03Y536D
  • 04Y523D
  • 02Y522D
  • 02Y519D
  • 02Y512D
  • 01Y512D
  • 01Y511D
  • 02Y510D
  • 01Y505D
  • 02Y504D
  • 04Y355D
  • 02Y355D
  • 01Y352D
  • 01Y349D
  • 03Y348D
  • 01Y348D
  • 02Y348D
  • 01Y339D
  • 01Y335D
  • 02Y334D
  • 02Y335D
  • 03Y314D
  • 01Y313D
  • 02Y312D
  • 01Y312D
  • 02Y311D
  • 01Y311D
  • 02Y310D
  • 04Y310D
  • 02Y307D
  • 03Y307D
  • 01Y304D
  • 02Y303D
  • 02Y304D
71701-01357599000226
  • 01Y702D
  • 01Y694D
  • 03Y693D
  • 02Y686D
  • 03Y683D
  • 02Y574D
  • 01Y563D
  • 02Y563D
  • 01Y564D
  • 03Y562D
  • 01Y552D
  • 02Y552D
  • 06Y550D
  • 05Y539D
  • 05Y538D
  • 06Y537D
  • 01Y536D
  • 01Y532D
  • 02Y531D
  • 03Y522D
  • 02Y518D
  • 02Y511D
  • 01Y508D
  • 02Y505D
  • 04Y356D
  • 01Y356D
  • 02Y356D
  • 01Y321D
  • 01Y320D
  • 02Y320D
  • 01Y317D
  • 02Y317D
71739-01357599000240
  • 03Y754D
  • 03Y734D
  • 01Y705D
  • 01Y671D
Amount recalled
336,085

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

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, swelling, too hot to hold, it will no longer hold charge, or it fails Reader Test. Do not use other chargers. User Manual update includes instructions on reader safe storage, charging, use.

Using this product could cause serious injury, illness or death — stop using it now.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.