Globus Medical recalls

Globus Medical has 29 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 30 Apr 2025. 6 are still ongoing. The most frequent reason is foreign material.

Total recalls29since 2013
Last 12 months0reported
Class I13% of total
Ongoing6latest 30 Apr 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 3%Class II 28 97%Class III 0 0%

Why globus medical is recalled

By year

Ongoing globus medical recalls

6 active

All globus medical recalls, newest first

29 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIMagec 2 Rod Standard recalled by Globus MedicalGlobus MedicalOtherNationwide
DeviceCLASS IICranial Drill with Stop - instruments for access recalledGlobus MedicalSterilityNationwide
DeviceCLASS IICranial Drill with Stop - Instruments for access recalledGlobus MedicalSterilityNationwide
DeviceCLASS IICranial Drill - instruments for access, preparation recalledGlobus MedicalSterilityNationwide
DeviceCLASS IIExcelsiusGPS Cannula A, Cannula used with ball tip probes recalledGlobus MedicalSterilityNationwide
DeviceCLASS IExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit recalledGlobus MedicalLabeling Errors5 states
DeviceCLASS IIAltera Spacer Altera Spacer, 12-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 8-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 12-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 10-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 10-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 9-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 10-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 10-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 9-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 8-, 8¿ (sterile) recalledGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 9-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 9-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 8-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 12-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 9-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 10-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 9-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 12-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 8-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 12-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 12-, 8¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIAltera Spacer Altera Spacer, 10-, 15¿ recalled by Globus MedicalGlobus MedicalForeign MaterialPA
DeviceCLASS IIMicroFuse Putty, 2.5cc and 10cc recalled by Globus MedicalGlobus MedicalSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.