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Hermia OLINDA

Hermes Medical Solutions AB · Model 00859873006219 · UDI-DI 00859873006219

IYX Prescription

510(k) clearances

404

Adverse events (5 deaths)

Recalls

Facilities

Description

OLINDA/EXM® is a software application for nuclear medicine. Based on user input of time integrated activity in separate organs, OLINDA/EXM® calculates the organ dose and the whole-body dose and presents the results to the user. The results can be stored for future analysis. The dose estimates provided by OLINDA/EXM® may guide the decision making for future patient radionuclide therapy treatments or inform radiation protection measures for diagnostic radiopharmaceuticals.

Recalls

Date	Firm	Reason
2025-12-10	GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING	GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affecte
2025-12-10	GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING	GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affecte
2016-08-05	Siemens Medical Solutions USA, Inc.	"We have received reports of patients hair being caught in the e.cam and Symbia E patient bed up/down drive. The purpose of this letter is to remind users of the patient positionin
2004-07-30	General Electric Med Systems	The detector head of a FX-80 Nuclear camera may fall from the gantry. Three potential causes have been determined. (1) A ball nut in the detector's radial drive assembly can back
2004-07-30	General Electric Med Systems	The detector head of a FX-80 Nuclear camera may fall from the gantry. Three potential causes have been determined. (1) A ball nut in the detector's radial drive assembly can back
2004-01-16	GVI Technology Partners	Due to limitations in the operating software, the acquired scan may not be processed properly.
2003-02-10	Siemens Medical Solutions USA, Inc.	Unintended yoke rotational motion.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.