Medtronic Xomed, Inc. Product is a surgical nasal/sinus surgical device labeled as a RAD Frontal Finesse Bur, Reference Number 18-83070 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Product is a surgical nasal/sinus surgical device labeled as a RAD Frontal Finesse Bur, Reference Number 18-83070
Brand
Medtronic Xomed, Inc.
Lot Codes / Batch Numbers
Lot 26371200
Products Sold
Lot 26371200
Medtronic Xomed, Inc. is recalling Product is a surgical nasal/sinus surgical device labeled as a RAD Frontal Finesse Bur, Reference Nu due to The curve in the shaft of the bur was only 15 degrees not the labeled 40 degrees.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The curve in the shaft of the bur was only 15 degrees not the labeled 40 degrees.
Recommended Action
Per FDA guidance
A Recall notification letter was mailed to each hospital account on January 29, 2004 for each type of device they received which was under recall explaining the error and asking the accounts to remove recalled product from inventory, fax them the response sheet and to return the products.
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
FL, ID, IN, LA, MA, MO, NJ, NY, NC, OK, TN, TX, UT, WI, WY
Page updated: Jan 10, 2026