Reported Jan 21, 2026 · Ongoing

FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component…

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 3
  • Plus Sensor REF 78769-01 UDI-DI code00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System
Lot codes and dates
  • Model Number78769-01
  • UDI-DI Code00357599843014
  • Product Expiry Date01/31/2026
  • Kit Pack Lot NumberT60003166
  • Pack Serial Numbers

    3,247 of 3,247 codes

    • 0HPCMWH9Y
    • 0HPCMWHAV
    • 0HPCMWHA9
    • 0HPCMWHA0
    • 0HPCMWHAK
    • 0HPCMWHAR
    • 0HPCMWHAU
    • 0HPCMWHAJ
    • 0HPCMWHAG
    • 0J8A08TUA
    • 0HPCMWHAQ
    • 0HPCMWHAF
    • 0J8A08TTZ
    • 0J8A08TUD
    • 0HPCMWHAT
    • 0J8A08TTY
    • 0J8A08TU1
    • 0HPCMWHAZ
    • 0J8A08TUC
    • 0J8A08TU0
    • 0HPCMWHC9
    • 0HPCMWHAX
    • 0J8A08TUE
    • 0J8A08TU2
    • 0HPCMWHAM
    • 0J8A08TUG
    • 0HPCMWHAW
    • 0HPCMWHAL
    • 0J8A08TU5
    • 0J8A08TUJ
    • 0HPCMWHAY
    • 0J8A08TU3
    • 0J8A08TU8
    • 0HPCMWHC4
    • 0J8A08TUH
    • 0J8A08TU7
    • 0HPCMWHL8
    • 0J8A08TW4
    • 0HPCMWHLL
    • 0HPCMWHL9
    • 0J8A08U3T
    • 0J8A08U45
    • 0J8A08TW3
    • 0J8A08U3U
    • 0J8A08U3Q
    • 0J8A08U3N
    • 0J8A08TW5
    • 0J8A08U3R
    • 0J8A08U3C
    • 0J8A08U3L
    • 0J8A08TW1
    • 0J8A08U39
    • 0J8A08U31
    • 0J8A08U3M
    • 0J8A08U3A
    • 0J8A08U2Q
    • 0J8A08U2Z
    • 0J8A08U3K
    • 0J8A08U2N
    • 0J8A08U3H
Amount recalled
258,913 sensors

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

Stop using this product now

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

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

Want the full recall guide?

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, 4:55 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.