FDASeptember 16, 2025device

Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding model numbers: 1. SPACER 6068073 CATALYFT PL SHORT 7MM. Model Number: 6068073. 2. SPACER 6068076 CATALYFT PL LONG 7MM, Model Number: 6068076. 3. SPACER 6068093 CATALYFT PL SHORT 9MM, Model Number: 6068093. 4. SPA...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury. Therefore, surgical technique and instructions for use will be updated to mitigate risk of loss of lordosis to occur.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic sofamor danekmedtronicmedtronic sofamor

UPCs

007630002466930076300052956700763000246709007630005295740076300024672300763000529581007630002467300076300052959800763000246754007630005296040076300024676100763000529611

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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