FDAApril 15, 2024device

MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT (single photon emission computerized tomography system).

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

The hazard

There is a potential issue regarding the service handles for the internal lead (Pb) covers in that the handles could loosen or release which could cause a cover to drop potentially resulting in injury to service personnel due to the weight of the cover.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems israel functional imaging

UPCs

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Recall history

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

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MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT (single photon emission computerized tomography system). — Recall Details · AllClear