Data Foundry

Medical device recalls 2013

Mizuho Orthopedic Table — Class II medical device recall Z-0810-2013

Terminated recall by Mizuho OSI, reported 2013-02-20, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Possible instability of Orthopedic Table Top. If the epoxy bond fails, the aluminum plug may migrate out of th

Recall numberZ-0810-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMizuho OSI, Union City, CA, United States
Recall initiated2012-12-17
Classified2013-02-13
Reported by FDA2013-02-20
Terminated2016-04-15
DistributedAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, WY
Countries outside the USAE, AU, CA, CN, DE, EG, ES, FI, FR, GB, IL, IT, JP, KR, NL, NZ, SA, SG, SI, TW
Quantity869 devices
Reason classesspecification failure
Model numbers5855

Product

Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.

Reason for recall

Possible instability of Orthopedic Table Top. If the epoxy bond fails, the aluminum plug may migrate out of the carbon fiber tube. If this occurs, the Orthopedic Table Spar may need to be replaced to ensure stability of the Orthopedic Table Top.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0810-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.