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Achilles EXPII

GE Medical Systems (China) Co.,Ltd. · Model v1 · UDI-DI 00840682116978

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

Description

BONE ULTRASONOMETER, ACHILLES

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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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.