Medtronic Xomed, Inc. The product is a sheath meant to fit over a Nasopharyngoscope and is labeled as EndoScrub 2 Sheaths Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The product is a sheath meant to fit over a Nasopharyngoscope and is labeled as EndoScrub 2 Sheaths
Brand
Medtronic Xomed, Inc.
Lot Codes / Batch Numbers
Lots 31396400 and 30722300
Products Sold
Lots 31396400 and 30722300
Medtronic Xomed, Inc. is recalling The product is a sheath meant to fit over a Nasopharyngoscope and is labeled as EndoScrub 2 Sheaths due to The sheaths in question have shafts that are one inch longer than required for the endoscope specified on the label.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The sheaths in question have shafts that are one inch longer than required for the endoscope specified on the label.
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