Vertier Surgical Table, an AC powered, general purpose, mobile surgical table with electro-hydraulically controlled move
FDA device recall Z-1899-2009 · posted 2009-08-26 · Terminated
Recall details
- Recalling firm
- Stryker Communications Corp
- Reason for recall
- Surgical tables were produced using an unapproved tilt frame bushing.
- Action taken
- 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.
- Root cause
- Nonconforming Material/Component
- Status
- Terminated
- Product code
- FQO
- Quantity affected
- 31
- Distribution
- Worldwide Distribution -- United States (OR, IL, WA, CA, AR, TX, UT, SC and GA) and Canada.
- Date initiated
- 2008-11-13
- Date posted
- 2009-08-26
- Date terminated
- 2009-08-28
- Location
- Flower Mound, TX
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