Stryker Spine LITe Decompression Snake Arm, REF 48080230 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LITe Decompression Snake Arm, REF 48080230
Brand
Stryker Spine
Lot Codes / Batch Numbers
UDI-DI (GTIN): 07613327263909, lot # 227764.
Products Sold
UDI-DI (GTIN): 07613327263909, lot # 227764.
Stryker Spine is recalling LITe Decompression Snake Arm, REF 48080230 due to Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Recommended Action
Per FDA guidance
Stryker issued Urgent Medical Device Correction on 11/20/2023 notifying customers of removal of lot 227764 of the LITe Decompression Tube Snake Arm, catalog number 48080230. A portion of one lot of the LITe Decompression Tube Snake Arm was manufactured with the incorrect clamp component. As a result, the affected Snake Arms cannot attach to the arm post shaft. Customers are to review inventory and remove units from points of use for return to Stryker, share this information with appropriate personnel and return the Business Reply form to Spine-RegulatoryActions@Stryker.com. If you have any questions or concerns, please contact Regulatory Compliance at (201) 749-8090.
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 noticeDistribution
As reported by FDA
MD, MI, NM, TX
Page updated: Jan 10, 2026