Device recall

Z-0995-2024: Globus Medical Cranial Drill with Stop, 2.40mm - Instruments for access…

FDA device recall · Class II · Globus Medical, Inc.

Key facts

Recall number (Z-number) Z-0995-2024
Recall event 93742
Product Globus Medical Cranial Drill with Stop, 2.40mm - Instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref : 6143.1834S
Product code HAW
Recalling firm Globus Medical, Inc.
Recall class Class II
Status Open, Classified
510(k) numbers K200047
FEI number 3004142400

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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