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FDA (Device enforcement)Recalled 2024-07-03class ii

Siemens Medical Solutions USA, Inc: Sensis Vibe systems with software version VD15B in combination with VM VIRTUAL SERVER Model: 10765502-Intended to be used as a diagnostic and administrative tool su

Hazard

If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash.

Details from the source

Reason for recall: If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash. Distribution: US Nationwide distribution in the states of CA, CT, FL, IA, KS, MA, MI, NJ, TX, VA. Quantity: 7 systems Lot/code info: UDI-DI: N/A Serial Numbers: Serial 18023 18022 18020 18021 18019 18025 18017

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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