--- title: "Catalyft PL & PL40 Expandable Interbody System labeled as follows with corres... — FDA record Z-0580-2026 | Is It on Recall" description: "Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury. Theref" url: https://isitonrecall.com/recall/fda-device-z-0580-2026-catalyft-pl-pl40-expandable-interbody-system-labeled-as-follows-with-corresponding-model-numbers-1-s/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding model numbers: 1. SPACER 6068073... — FDA record Z-0580-2026 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Sep 16, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: 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. SPACER 6068096 CATALYFT PL LONG 9MM, Model Number: 6068096. 5. SPACER 6068113 CATALYFT PL SHORT 11MM, Model Number: 6068113. 6. SPACER 6068116 CATALYFT PL LONG 11MM, Model Number: 6068116. 7. SPACER 6069073 CATALYFT PL40 SHORT 7MM, Model Number: 6069073. 8. SPACER 6069076 CATALYFT PL40 LONG 7MM, Model Number: 6069076. 9. SPACER 6069093 CATALYFT PL40 SHORT 9MM, Model Number: 6069093. 10. SPACER 6069096 CATALYFT PL40 LONG 9MM, Model Number: 6069096. 11. SPACER 6069113 CATALYFT PL40 SHORT 11MM, Model Number: 6069113. 12. SPACER 6069116 CATALYFT PL40 LONG 11MM, Model Number: 6069116. 13. CATALYFT PL IMPLANT SET, Model Number: SPS03143. 14. CATALYFT PL 40 IMPLANT SET, Model Number: SPS03144. 15. KIT CATALYFT PL IMPLANTS, Model Number: SPS04012. 16. KIT CATALYFT PL 40 IMPLANTS, Model Number: SPS04013. 17. CATALYFT PL 40 IMP KIT, Model Number: SPSJEP40. 18. CATALYFT PL 40 HIGH IMP KIT, Model Number: SPSJEP4H. 19. CATALYFT PL 40 SHORT IMP KIT, Model Number: SPSJEP4S. 20. CATALYFT PL 40 SHORT HIGH IMP KIT, Model Number: SPSJEP4T. 21. CATALYFT PL STRAIGHT HIGH IMP KIT, Model Number: SPSJEPSH. 22. CATALYFT PL STRAIGHT IMP KIT, Model Number: SPSJEPSI. These systems utilize the following affected Instructions for Use (IFU), Document M333023W048E, and Surgical Technique Guide, Document M333023W217. - **Reason**: 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. - **Classification**: Class II - **Recalling firm**: Medtronic Sofamor Danek USA Inc - **Quantity**: 275,260 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-0580-2026 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0580-2026%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | IFU: M333023W048E Rev. A Surgical TechniqueM333023W217, Rev. 2.0 1. Model Number: 6068073. 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0999209W, 1000720W, 1002203W, 1002209W, 1003055W, 1003059W, 1003061W, 1003068W, 1003590W, 1004007W, 1005095W, 1006066W, 1006608W, 1007435W, 1007561W, 1007567W, 1007569W, 1008574W, 1008578W, 1008907W, 1008909W, 1009421W, 1009425W, 1009431W, 1010466W, 1010542W, 1010550W, 1010552W, 1012752W, 1013085W, 1016350W, 1016356W, 1017284W, 1017288W, 1017294W, 1018228W, 1018232W, 1018236W, 1018324W, 1018326W, 1018658W, 1019499W, 1020114W, 1020116W, 1020120W, 1020513W, 1021729W, 1021767W, 1023316W, 1024213W, 1024215W, 1024217W, 1025154W, 1025160W, 1026564W, 1026570W, 1026825W, 1027612W, 1028545W, 1028547W, 1028704W, 1034570W, 1035141W, 1035145W, 1035149W, 1035151W, 1035155W, 1035157W, 1035159W, 1035161W, 1036542W, 1037691W, 1037693W, 1038210W, 1038250W, 1039194W, 1039592W, 1040466W, 1040468W, 1042955W, 1042959W, 1042963W, 1043672W, 1043676W, 1044340W, 1044589W, 1044641W, 1044717W, 1045694W, 1046302W, 1046304W, 1046306W, 1047619W, 1048281W, 1048283W, 1048285W, 1048289W, 1048291W, 1048293W, 1048882W, 1050572W, 1050574W, 1050576W, 1050578W, 1050580W, 1050584W, 1050586W, 1050590W, 1050592W, 1052420W, 1056849W, 1057484W, 1057486W, 1059122W, 1059124W, 1059126W, 1059128W, 1059673W, 1059679W, 1059681W, 1060018W, 1060042W, 1061132W, 1061136W, 1061138W, 1061140W, H5962482, H5969220, H5979175, H5979177, H5980995, H5981839, H5983795, H5991698, H5993288, H6018660, H6024652, H6030042, H6032572, H6040357, 1002451W, 1008576W, 1040457W, 1056901W, H6028216). 2. Model Number: 6068076. GTIN (Lot Numbers): 00763000246709 (0831754W, 0836194W, 0836196W, 0837729W, 0842801W, 0844113W, 0848626W, 0851984W, 0852133W, 0852135W, 0854453W, 0855324W, 0858930W, 0860486W, 0862453W, 0869639W, 0869697W, 0870551W, 0873204W, 0873206W, 0874508W, 0877437W, 0879344W, 0879346W, 0879889W, 0881318W, 0881320W, 0881322W, 0881324W, 0888801W, 0891953W, 0891955W, 0891957W, 0891959W, 0891961W, 0893334W, 0895572W, 0896956W, 0896958W, 0897310W, 0900775W, 0901194W, 0902364W, 0903364W, 0904722W, 0906156W, 0907658W, 0910204W, 0910206W, 0914582W, 0917664W, 0920057W, 0920059W, 0922963W, 0924473W, 0928840W, 0929162W, 0931918W, 0933077W, 0933079W, 0933081W, 0935292W, 0935294W, 0936460W, 0937874W, 0939328W, 0940207W, 0940209W, 0941916W, 0943259W, 0943491W, 0943959W, 0947406W, 0948522W, 0948524W, 0951518W, 0952754W, 0952756W, 0954066W, 0954068W, 0955354W, 0955356W, 0955504W, 0955506W, 0957553W, 0957555W, 0959042W, 0959044W, 0961522W, 0962116W, 0962118W, 0962120W, 0962772W, 0962774W, 0967197W, 0967199W, 0967201W, 0969067W, 0973085W, 0974331W, 0974333W, 0975730W, 0976604W, 0976606W, 0976608W, 0976610W, 0976742W, 0978655W, 0978657W, 0980758W, 0980760W, 0980762W, 0983624W, 0986390W, 0989391W, 0992001W, 0992003W, 0992005W, 0992007W, 0992009W, 0993274W, 0993628W, 0993630W, 0995670W, 1002345W, 1002455W, 1002457W, 1003070W, 1003602W, 1004292W, 1004294W, 1004648W, 1004650W, 1005202W, 1007162W, 1007164W, 1007166W, 1007168W, 1007170W, 1007172W, 1007174W, 1007573W, 1007575W, 1007577W, 1007579W, 1007581W, 1007583W, 1010252W, 1010254W, 1010256W, 1010258W, 1010260W, 1010262W, 1010264W, 1010729W, 1011392W, 1011394W, 1011396W, 1011904W, 1011906W, 1013087W, 1013089W, 1013091W, 1013093W, 1013095W, 1013097W, 1013099W, 1014066W, 1014068W, 1014070W, 1014072W, 1014074W, 1014856W, 1014858W, 1014860W, 1015566W, 1015568W, 1015570W, 1015572W, 1015574W, 1015576W, 1015578W, 1016360W, 1018664W, 1018666W, 1019189W, 1019441W, 1019443W, 1019445W, 1019447W, 1019449W, 1020208W, 1020210W, 1020212W, 1020214W, 1020216W, 1020218W, 1021427W, 1021429W, 1021471W, 1021473W, 1021475W, 1021769W, 1022752W, 1024223W, 1025162W, 1026251W, 1026829W, 1027614W, 1027616W, 1027618W, 1027620W, 1028551W, 1030261W, 1031319W, 1031331W, 1031333W, 1031496W, 1031498W, 1031500W, 1031682W, 1032064W, 1032066W, 1032068W, 1032581W, 1032583W, 1032585W, 1033164W, 1033166W, 1033168W, 1033170W, 1033172W, 1033934W, 1034572W, 1034574W, 1034576W, 1034578W, 1034582W, 1034584W, 1036020W, ... | The agency lot list is longer than this excerpt. [Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0580-2026%22). Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Worldwide distribution - US Nationwide and Puerto Rico. The countries of Australia, Austria, Belgium, Canada, Croatia, Czech Republic, Denmark, France, Germany, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Netherlands, New Caledonia, New Zealand, Norway, Portugal, Reunion, Saudi Arabia, Singapore, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom. States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address. - [Alaska](https://isitonrecall.com/state/alaska/) - [Alabama](https://isitonrecall.com/state/alabama/) - [Arkansas](https://isitonrecall.com/state/arkansas/) - [Arizona](https://isitonrecall.com/state/arizona/) - [California](https://isitonrecall.com/state/california/) - [Colorado](https://isitonrecall.com/state/colorado/) - [Connecticut](https://isitonrecall.com/state/connecticut/) - [Delaware](https://isitonrecall.com/state/delaware/) - [Florida](https://isitonrecall.com/state/florida/) - [Georgia](https://isitonrecall.com/state/georgia/) - [Hawaii](https://isitonrecall.com/state/hawaii/) - [Iowa](https://isitonrecall.com/state/iowa/) - [Idaho](https://isitonrecall.com/state/idaho/) - [Illinois](https://isitonrecall.com/state/illinois/) - [Indiana](https://isitonrecall.com/state/indiana/) - [Kansas](https://isitonrecall.com/state/kansas/) - [Kentucky](https://isitonrecall.com/state/kentucky/) - [Louisiana](https://isitonrecall.com/state/louisiana/) - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Maryland](https://isitonrecall.com/state/maryland/) - [Maine](https://isitonrecall.com/state/maine/) - [Michigan](https://isitonrecall.com/state/michigan/) - [Minnesota](https://isitonrecall.com/state/minnesota/) - [Missouri](https://isitonrecall.com/state/missouri/) - [Mississippi](https://isitonrecall.com/state/mississippi/) - [Montana](https://isitonrecall.com/state/montana/) - [North Carolina](https://isitonrecall.com/state/north-carolina/) - [North Dakota](https://isitonrecall.com/state/north-dakota/) - [Nebraska](https://isitonrecall.com/state/nebraska/) - [New Hampshire](https://isitonrecall.com/state/new-hampshire/) - [New Jersey](https://isitonrecall.com/state/new-jersey/) - [New Mexico](https://isitonrecall.com/state/new-mexico/) - [Nevada](https://isitonrecall.com/state/nevada/) - [New York](https://isitonrecall.com/state/new-york/) - [Ohio](https://isitonrecall.com/state/ohio/) - [Oklahoma](https://isitonrecall.com/state/oklahoma/) - [Oregon](https://isitonrecall.com/state/oregon/) - [Pennsylvania](https://isitonrecall.com/state/pennsylvania/) - [Rhode Island](https://isitonrecall.com/state/rhode-island/) - [South Carolina](https://isitonrecall.com/state/south-carolina/) - [South Dakota](https://isitonrecall.com/state/south-dakota/) - [Tennessee](https://isitonrecall.com/state/tennessee/) - [Texas](https://isitonrecall.com/state/texas/) - [Utah](https://isitonrecall.com/state/utah/) - [Virginia](https://isitonrecall.com/state/virginia/) - [Vermont](https://isitonrecall.com/state/vermont/) - [Washington](https://isitonrecall.com/state/washington/) - [Wisconsin](https://isitonrecall.com/state/wisconsin/) - [West Virginia](https://isitonrecall.com/state/west-virginia/) - [Wyoming](https://isitonrecall.com/state/wyoming/) ## Dates in the source - **Report date**: Dec 3, 2025 - **Recall initiation date**: Sep 16, 2025 - **Center classification date**: Nov 21, 2025 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0580-2026%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Sofamor Danek USA Inc records](https://isitonrecall.com/brand/medtronic-sofamor-danek-usa-inc/)