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Recall Observatory FDA recall evidence

Device product

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.

Z-0091-2021

October 14, 2019

Class II

Product summary

Firm
Mizuho OSI
Event
Event 86482
Status
Terminated
Classification
Class II
Quantity
174 Arms
Official record key
device-enforcement:Z-0091-2021

Official wording

Reason: 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

Code information: Model Number: 7887-050 UDI/GTIN 00842230104992 Affected Serial Numbers: 201 through 452 Model 7887-050R UDI/GTIN 00824230108440 Affected Serial Numbers: 234, 235, 248, 255, 341, and 448

Distribution pattern: Worldwide distribution - U.S. Nationwide distribution including in states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, LA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, NV, OH, OK, OR, PA, SC, TN, TX, VA, WI, and WV. The countries of Australia, Belgium, Canada, Columbia, Germany, Israel, South Korea, New Zealand, Poland, United Kingdom, and South Africa.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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