FDA Recalls Mizuho OSI Modular Table Systems Due to Patient Falls

The U.S. Food and Drug Administration has issued a Class I Recall of Mizuho OSI Modular Table Systems following reports of patient injury.

The Mizuho OSI Modular Table Systems are used to position patients during orthopedic trauma, thoracic and spinal surgery procedures. The FDA has received reports of patient falls from the table due to incorrect removal of the T-pins that support the bottom base and unexpected movement/tilting of the table.

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