Stryker Spine Radius Rod Persuader is a non-sterile instrument for use with other devices in spinal surgery. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Radius Rod Persuader is a non-sterile instrument for use with other devices in spinal surgery.
Brand
Stryker Spine
Lot Codes / Batch Numbers
Lot Codes 067805, 067806, 067807, 06D694. Catalog number: 486619190
Products Sold
Lot Codes 067805, 067806, 067807, 06D694. Catalog number: 486619190
Stryker Spine is recalling Radius Rod Persuader is a non-sterile instrument for use with other devices in spinal surgery. due to The t-bar of the Radius Rod Persuader devices froze due to a loosening screw causing the device to fail.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The t-bar of the Radius Rod Persuader devices froze due to a loosening screw causing the device to fail.
Recommended Action
Per FDA guidance
Recall notification was sent via FedEx on February 19, 2008 to all branches/agencies. All questions are to be directed to Michelle Klein, Regulatory Compliance Specialist - 201-760-8256.
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