LITe Decompression Snake Arm, REF 48080230
FDA Recall Z-0610-2024 · Posted 2023-12-21
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Recalling FirmStryker Spine
Recall StatusOpen, Classified
Product CodeLXH
Date Initiated2023-11-01
Product Quantity9
Reason for Recall
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Firm Action
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 [email protected]. If you have any questions or concerns, please contact Regulatory Compliance at (201) 749-8090.
Root Cause
Nonconforming Material/Component
Distribution Pattern
US: MD, MI, NM, TX & OUS: Canada & France.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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