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Echolight S.p.a.

ECHOLIGHT SPA · Model EchoStation · UDI-DI 08052461860053

MUAOMV Prescription
1
510(k) clearances
1
Adverse events
2
Recalls
6
Facilities

Recalls

DateFirmReason
2019-09-03GE Healthcare, LLCCertain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective
2019-09-03GE Healthcare, LLCCertain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.