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FDANovember 18, 2022device

MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1

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

The hazard

Stryker received a report of a battery fire involving an Airo TruCT unit previously subjected to bypass charging. The firm is notifying customers with units whose battery monitoring systems were bypassed to charge the batteries; the batteries in these units require replacing.

What to do

FDA enforcement status: Terminated

Brands named

mobius imagingmobius

UPCs

00869346000200

Recall history

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

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MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1 — Recall Details · AllClear