FDAJuly 19, 2019device

Aestiva 7900, Model Numbers: a) 1006-9300-000 b) 1006-9305-000 c) 1006-9118-000 d) 1006-9112-000 e) 1006-9113-000 f) 1006-9020-000 g) 1006-9033-000 h) 1006-9117-000 i) 1006-9119-000 j) 1006-9030-000 k) 1006-9032-000 l) 1006-9022-000 m) To be provided n) 1006-9120-000 o) 1006-9027-000 p) 1006-9003...

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

The hazard

Certain Aespire and Aestiva Anesthesia Systems were noted to have a vulnerability to a cyber-attack when connected to the hospital network. An insufficiently secured terminal server may provide an opportunity for a malicious actor that has already penetrated the hospital network to send fraudulent flow sensor correction parameters.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

UPCs

100693000001006930500010069118000100691120001006911300010069020000100690330001006911700010069119000100690300001006903200010069022000

Recall history

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

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