Z-1238-2010

Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S

Name: Z-1238-2010 Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S
Creator: Stryker Communications Corp
Published: 2009-11-13
License: https://open.fda.gov/license/

STRYKER Communications, Inc. / initiated 2009-11-13 / Terminated

FDA source

Stryker Communications Corp began a recall of Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S on 2009-11-13. The reason FDA records is "In certain positions, product is susceptible to fluid instrusion which could possibly result in short circuit or unsolicited movement". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1238-2010
Status: Terminated
Initiated: 2009-11-13
Posted: 2010-04-06
Terminated: 2010-08-11
Recalling firm: STRYKER Communications, Inc.
Product: Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S
Product code: FQO Table, Operating-Room, Ac-Powered
Reason for recall: In certain positions, product is susceptible to fluid instrusion which could possibly result in short circuit or unsolicited movement.
FDA root cause: Other
Action: Firm notified all consignees by letter sent 11/13/2009. Contact the firm at 972-410-7100 with questions relating to this recall.
Quantity in commerce: 206
Distribution: United States (GA, AR, ND, KY, CO, CA, SD, PA, OH, TX, SC, NY, MS, IL, KS, NJ, OR, WA, MN, VA, IL, OK, WY, IN, ID, UT, MO, FL, and DC) and Canada.
Product codes and lots: All Lots Are Affected

Product code FQO

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)