Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Recalled by Mizuho OSI Due to Due to the potential for fluid ingress into...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mizuho OSI directly.
Affected Products
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.
Quantity: 174 Arms
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mizuho OSI
Mizuho OSI has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report