Stryker Spine Reflex Revision Screwdriver Inner Shaft is a orthopedic manual surgical instrument that is a nonpowered, hand held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. Ref Number 48500900;Non Sterile Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Reflex Revision Screwdriver Inner Shaft is a orthopedic manual surgical instrument that is a nonpowered, hand held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. Ref Number 48500900;Non Sterile
Brand
Stryker Spine
Lot Codes / Batch Numbers
Lot codes: 26719, 047377, 047570, 065167, 06A167, and 072689.
Products Sold
Lot codes: 26719, 047377, 047570, 065167, 06A167, and 072689.
Stryker Spine is recalling Reflex Revision Screwdriver Inner Shaft is a orthopedic manual surgical instrument that is a nonpowe due to The Inner Shaft does not extend far enough from the tip of the Revision Screwdriver to fully engage the bone screw.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Inner Shaft does not extend far enough from the tip of the Revision Screwdriver to fully engage the bone screw.
Recommended Action
Per FDA guidance
URGENT PRODUCT RECALL letters were sent to all branches/agencies who received the product on June 5, 2008. If you have questions, contact Michelle Klein at 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