Stryker Spine Radius Capspin 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 Capspin is a non-sterile instrument for use with other devices in spinal surgery.
Brand
Stryker Spine
Lot Codes / Batch Numbers
06A277, 06A279, 06D632 Catalog number: 486619210
Products Sold
06A277, 06A279, 06D632 Catalog number: 486619210
Stryker Spine is recalling Radius Capspin is a non-sterile instrument for use with other devices in spinal surgery. due to The Radius Capsin has separation of the tip from the inserter.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Radius Capsin has separation of the tip from the inserter.
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