Stryker Howmedica Osteonics Corp. The TRIO Spondylolisthesis Reduction Instrument is a Class I Manual Surgical Instrument unique to the implantation of Stryker Spine TRIO PS this instrument is intended for use in the reduction of degenerative Spondylolisthesis. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The TRIO Spondylolisthesis Reduction Instrument is a Class I Manual Surgical Instrument unique to the implantation of Stryker Spine TRIO PS this instrument is intended for use in the reduction of degenerative Spondylolisthesis.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog No: 48905110 Lot Code: 039524, 039981, 045152, 045153, 045154, 045155, 045156, 045157, 045158, 045159, 048721, 048722.
Products Sold
Catalog No: 48905110 Lot Code: 039524; 039981; 045152; 045153; 045154; 045155; 045156; 045157; 045158; 045159; 048721; 048722.
Stryker Howmedica Osteonics Corp. is recalling The TRIO Spondylolisthesis Reduction Instrument is a Class I Manual Surgical Instrument unique to th due to The threaded part of the instrument may break when connected to the screw and potentially result in an adverse health consequence.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The threaded part of the instrument may break when connected to the screw and potentially result in an adverse health consequence.
Recommended Action
Per FDA guidance
The notification letters and product accountability forms were sent to their branches/agencies and the one hospital via Fedex on 5/16/2005 with return receipt.
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