Medtronic Surgical Navigation Technologies, Inc Stealth Station Cranial Application v.4.5 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stealth Station Cranial Application v.4.5
Brand
Medtronic Surgical Navigation Technologies, Inc
Lot Codes / Batch Numbers
Catalog Numbers: 960-201 and 9730888. Cranial Application software v.4.5.
Products Sold
Catalog Numbers: 960-201 and 9730888. Cranial Application software v.4.5.
Medtronic Surgical Navigation Technologies, Inc is recalling Stealth Station Cranial Application v.4.5 due to The Stealth Station Cranial Application Version 4.5 contains a software anomaly, which may present a hazard to the patient.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Stealth Station Cranial Application Version 4.5 contains a software anomaly, which may present a hazard to the patient.
Recommended Action
Per FDA guidance
Customers were sent notification letters dated 01/28/05 and 02/02/05.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, FL, GA, IL, LA, MT, NV, NY, NC, ND, OH, OK, OR, PA, TX, VA, WA, WI, WY
Page updated: Jan 10, 2026