FDA Medical Device Recalls (openFDA)
Stryker Communications Corp: Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S
- Recall number
- Z-1238-2010
- Recalling firm
- Stryker Communications Corp
- Product
- Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S
- Status
- Terminated
- Initiated
- 2009-11-13
- Posted
- 2010-04-06
- Terminated
- 2010-08-11
- Reason
- In certain positions, product is susceptible to fluid instrusion which could possibly result in short circuit or unsolicited movement.
- 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
- 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.
- Lot, serial or model codes
- All Lots Are Affected
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FQO
- Firm FEI
- 3002975342
- Firm city
- Flower Mound
- Firm state
- TX
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28