Stryker Communications Corp Vertier Surgical Table, an AC powered, general purpose, mobile surgical table with electro-hydraulically controlled movements which are part of a control feedback system. Part Numbers: 0788100000 Standard table, 0788100001 Standard table with 5th wheel, 0788100000S SIDNE-enabled standard table, and 0788100001S SIDNE-enabled 5th wheel table Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vertier Surgical Table, an AC powered, general purpose, mobile surgical table with electro-hydraulically controlled movements which are part of a control feedback system. Part Numbers: 0788100000 Standard table, 0788100001 Standard table with 5th wheel, 0788100000S SIDNE-enabled standard table, and 0788100001S SIDNE-enabled 5th wheel table
Brand
Stryker Communications Corp
Lot Codes / Batch Numbers
Lot Numbers: 080111-43525, 080111-43526, 080111-43527, 080111-43528, 080118-43529, 080118-43530, 080118-43531, 080118-43532, 080118-43533, 080118-43537, 080118-43538, 080811-54955, 080811-54956, 080811-54957, 080811-54958, 080811-54959, 080811-54961, 080811-54962, 080811-54963, 080811-54964, 080811-54965, 080811-54966, 080811-54967, 080811-54968, 080811-54985, 080811-54986, 080811-54987, 080811-54988, 080811-54989, 080811-54998 and 080811-55002.
Products Sold
Lot Numbers: 080111-43525, 080111-43526, 080111-43527, 080111-43528, 080118-43529, 080118-43530, 080118-43531, 080118-43532, 080118-43533, 080118-43537, 080118-43538, 080811-54955, 080811-54956, 080811-54957, 080811-54958, 080811-54959, 080811-54961, 080811-54962, 080811-54963, 080811-54964, 080811-54965, 080811-54966, 080811-54967, 080811-54968, 080811-54985, 080811-54986, 080811-54987, 080811-54988, 080811-54989, 080811-54998 and 080811-55002.
Stryker Communications Corp is recalling Vertier Surgical Table, an AC powered, general purpose, mobile surgical table with electro-hydraulic due to Surgical tables were produced using an unapproved tilt frame bushing.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Surgical tables were produced using an unapproved tilt frame bushing.
Recommended Action
Per FDA guidance
Stryker Communications issued an "Urgent: Medical Device Recall" notice dated November 13, 2008 informing Consignees of the affected product. The firm intends to contact each facility to coordinate service by a trained representative. For further information, contact Stryker at 1-972-410-7100.
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 noticePage updated: Jan 10, 2026