Medtronic Xomed, Inc. Product is a device used in adenoid surgery and is labeled as Lusk Disposable Adenoid Curettes. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Product is a device used in adenoid surgery and is labeled as Lusk Disposable Adenoid Curettes.
Brand
Medtronic Xomed, Inc.
Lot Codes / Batch Numbers
Lot 30685400
Products Sold
Lot 30685400
Medtronic Xomed, Inc. is recalling Product is a device used in adenoid surgery and is labeled as Lusk Disposable Adenoid Curettes. due to The box label indicates that the product is a size 2 whereas a size 4 was packed inside.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The box label indicates that the product is a size 2 whereas a size 4 was packed inside.
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