Data Foundry

Medical device recalls 2023

FreeStyle Libre Reader — Class I medical device recall Z-1275-2023

Ongoing recall by Abbott Diabetes Care, Inc., reported 2023-04-12, distributed nationwide. Lithium-ion batteries in glucose monitoring system readers may swell, overheat, or pose fire hazard. Only use

Recall numberZ-1275-2023
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAbbott Diabetes Care, Inc., Alameda, CA, United States
Recall initiated2023-02-13
Classified2023-04-06
Reported by FDA2023-04-12
DistributedNationwide (US)
Quantity1,534,532
Reason classespackaging, device malfunction
UPC / GTIN / UDI-DI00357599803001, 00357599804008, 00357599805005
Lot numbers01A198D, 01A202D, 01A204D, 01A206D, 01A210D, 01A211D, 01A219D, 01A220D, 01A223D, 01A224D, 01A231D, 01A252D, 01A253D, 01A254D, 01A255D, 01A256D, 01A258D, 01A259D, 01A260D, 01A267D, 01A272D, 01A273D, 01A281D, 01A283D, 01A289D, 01A290D, 01A296D, 01A301D, 01A302D, 01A308D, 01A311D, 01A316D, 01A322D, 01A328D, 01A330D, 01A343D, 01A346D, 01A352D, 01A364D, 01B007F and 444 more
Model numbers71951-01, 71952-01, 71953-01

Product

FreeStyle Libre Reader, REF: 71951-01, 71952-01, 71953-01 a component of the FreeStyle Libre 2 Flash Glucose Monitoring System

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1275-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.