FDAJuly 10, 2019device

ABL90 FLEX Analyzer REF 393090 UDI:05700693930909

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Software Security; The action is being initiated because of software security vulnerabilities with the firm's analyzer operating system, which may cause the device to shutdown or reboot resulting in delayed medical treatment.

What to do

FDA enforcement status: Terminated

Brands named

radiometer americaradiometer

UPCs

05700693930909

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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ABL90 FLEX Analyzer REF 393090 UDI:05700693930909 — Recall Details · AllClear