Smith And Nephew, Inc. Endoscopy Division Endocoupler C-Mount 35 mmFocal Length Catalog Number: 6900398 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Endocoupler C-Mount 35 mmFocal Length Catalog Number: 6900398
Brand
Smith And Nephew, Inc. Endoscopy Division
Lot Codes / Batch Numbers
Serial #s: 50001621-2 50001621-1
Products Sold
Serial #s: 50001621-2 50001621-1
Smith And Nephew, Inc. Endoscopy Division is recalling Endocoupler C-Mount 35 mmFocal Length Catalog Number: 6900398 due to Endocouplers assembled with screws that cannot be effectively sterilized. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Endocouplers assembled with screws that cannot be effectively sterilized
Recommended Action
Per FDA guidance
Smith & Nephew notified customers and sales rep. by letter dated 2/19/04. Sales reps will retrieve product and replace effected units in the field.
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, CA, CT, ME, MA, MI, MO, NH, NJ, NY, NC, OH, PA, TN, TX, UT, VT, WA
Page updated: Jan 10, 2026