Medtronic Sofamor Danek Usa, Inc.
1800 PYRAMID PLACE, Memphis, TN, US
Registered product codes
118 product codes
Recent MDR events
24,161 on file
- KYPHON® HV-R® Bone CementJul 31, 2026Malfunction3003120897-2026-01312
- SOVEREIGNJul 31, 2026Malfunction3003120897-2026-01313
- ARTiC-L¿ and ARTiC-XL¿ Spinal SystemJul 31, 2026Malfunction3003120897-2026-01314
- ARTiC-L¿ and ARTiC-XL¿ Spinal SystemJul 31, 2026Malfunction3003120897-2026-01315
- PERIMETER¿ SystemJul 31, 2026Malfunction3003120897-2026-01316
- METRX IIJul 31, 2026Malfunction3003120897-2026-01317
- SEXTANTJul 31, 2026Malfunction3003120897-2026-01318
- METRx(TM) SystemJul 31, 2026Malfunction3003120897-2026-01319
- ANTERALIGN¿ Spinal System with Titan nanoLOCK¿ Surface TechnologyJul 31, 2026Malfunction3003120897-2026-01320
- KYPHON® HV-R® Bone CementJul 31, 2026Malfunction3003120897-2026-01321
Recalls
176 on file
- Open, ClassifiedNov 21, 2025
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.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedOct 25, 2023
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
View FDA record ↗ - Open, ClassifiedSep 8, 2023
The incorrect product labeling was applied to the product indicating the wrong size of product.
View FDA record ↗ - Open, ClassifiedAug 9, 2023
Incorrect Laser Marking - Solera Awl Tip Tap
View FDA record ↗
Compliance history
Matched by FEI 1000477302.
FDA inspections
1 on file
- No Action Indicated (NAI)Feb 6, 2026
Bioresearch Monitoring
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.