Mizuho Orthopedic Systems Inc OSI, 6822 IntraOp Series Tables, Operating Room tables, Orthopedic Systems, Inc., Union City, CA. (Series 6800 and 6822 included) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OSI, 6822 IntraOp Series Tables, Operating Room tables, Orthopedic Systems, Inc., Union City, CA. (Series 6800 and 6822 included)
Brand
Mizuho Orthopedic Systems Inc
Lot Codes / Batch Numbers
Serial Numbers: 12-15, 17, 19, 21-57, 59-61, 64-67, 70, 71, 73-83, 85-93, 95, 97, 99-134 and 136-141
Products Sold
Serial Numbers: 12-15, 17, 19, 21-57, 59-61, 64-67, 70, 71, 73-83, 85-93, 95, 97, 99-134 and 136-141
Mizuho Orthopedic Systems Inc is recalling OSI, 6822 IntraOp Series Tables, Operating Room tables, Orthopedic Systems, Inc., Union City, CA. (S due to Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.
Recommended Action
Per FDA guidance
The firm issued a Product Correction Notification letter by mail on 02/28/2007 and follow up with phone calls. The letter notified users that a required no-cost upgrade of the removal and replacement of a microprocessor that controls the logic for the floor locking mechanism will be conducted by the recalling firm.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, CA, FL, GA, HI, IL, IN, KS, KY, ME, MD, MA, MI, MO, NE, NH, NJ, NM, NY, NC, OH, OR, PA, SC, TX, VA, WA, WV, WI, WY
Page updated: Jan 10, 2026