Data Foundry

Medical device recalls 2014

FreeStyle Flash Blood Glucose Monitors System — Class I medical device recall Z-1212-2014

Terminated recall by Abbott Diabetes Care, Inc., reported 2014-03-26, distributed nationwide. Abbott Diabetes Care has identified through internal testing and investigation that all non-applied voltage le

Recall numberZ-1212-2014
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAbbott Diabetes Care, Inc., Alameda, CA, United States
Recall initiated2014-02-19
Classified2014-03-18
Reported by FDA2014-03-26
Terminated2015-08-11
DistributedNationwide (US)
Countries outside the USAT, CA, CH, DE, GB, IL, NL, NO, SE
Quantity25,203 units
NDC99073-0170-02
Model numbers17002

Product

FreeStyle Flash Blood Glucose Monitors System. Meter made in China; Distributed by TheraSense, Alameda, CA The FreeStyle Flash meter should only be used with FreeStyle Test Strips and FreeStyle Control Solution. Using other brands of test strips and control solutions with the FreeStyle Meter can product inaccurate results. Intended to monitor blood glucose from samples taken from the body. IVD use only,

Reason for recall

Abbott Diabetes Care has identified through internal testing and investigation that all non-applied voltage legacy meters have the potential to produce out of range control solution results and/or erroneously low blood glucose results when used in conjunction with Free Style test strips lots within expiry.

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-1212-2014. 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.