FDA Device recall Z-0810-2013
Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar
- FDA Device
- Class II
- terminated
- Published 2013-02-20
On 2013-02-20 the FDA classified a Class II recall of Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar by Mizuho Osi, citing 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 ne….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0810-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-12-17 |
| Published | 2013-02-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mizuho Osi |
| Distribution | AK, 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 |
Product
Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.
Reason
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.
Identifiers
| code_info | Table model 5855, sub assembly 5855-901 Orthopedic Table Spar, manufactured between 1996 and 2007. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0810-2013%22
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