Data Foundry

Medical device recalls 2024

Globus Medical Cranial Drill with Stop — Class II medical device recall Z-0996-2024

Ongoing recall by Globus Medical, Inc., reported 2024-02-14, distributed nationwide. Sterile-packed Cranial Drills may not be sterile due to a breach in the packaging and/or may have discoloratio

Recall numberZ-0996-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGlobus Medical, Inc., Audubon, PA, United States
Recall initiated2023-12-11
Classified2024-02-06
Reported by FDA2024-02-14
DistributedNationwide (US)
Countries outside the USCZ, PL
Reason classessterility
UPC / GTIN / UDI-DI00193982302269
Lot numbersGBY097GA, GBY097GA-RB, GBY097HA, GBY097HA-RB, GBY097JA, GBY097JA-RB, GBY097RA, GBY097RA-RB, GBY097VA, GBY097VA-RB
Model numbers6143.1842S

Product

Globus Medical Cranial Drill with Stop, 3.20mm - instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref: 6143.1842S

Reason for recall

Sterile-packed Cranial Drills may not be sterile due to a breach in the packaging and/or may have discoloration near the drill tip.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0996-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.