FDAOctober 14, 2019device

Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI - Product Usage: used with Mizuho OSI spinal surgery tables to provide patient head support and positioning during spinal surgery.

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

The hazard

Due to the potential for fluid ingress into the Arm which could affect the device's electrical system and lead to a failure of the locking mechanism

What to do

FDA enforcement status: Terminated

Brands named

mizuho osimizuho

UPCs

0084223010499200824230108440

Recall history

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

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