Smith And Nephew, Inc. Endoscopy Division Endocoupler , C-Mount 35 mm Focal Length Catalog Number: 7204614, 7204614M, 7204614S Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Endocoupler , C-Mount 35 mm Focal Length Catalog Number: 7204614, 7204614M, 7204614S
Brand
Smith And Nephew, Inc. Endoscopy Division
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Part No: 7204614 Serial #s: QW 17251 QW 17264 QW 17064 QW 17301 QW 17240 QW 17312 QW 17271 QW 17311 QW 17236 QW 17274 QW 17256 QW 17266 QW 16939 QW 17296 QW 17187 QW 17306 QW 17062 QW 17235 QW 17063 QW 17304 QW 17245 QW 17309 QW 17299 QW 17182 QW 17061 QW 17241 QW 17065 QW 17246 QW 17316 QW 17250 QW 16979 QW 17294 QW 16984 QW 17269 QW 17058 QW 17276 QW 17186 QW 17281 QW 17279 QW 17286 QW 17307 QW 17290 QW 16945 QW 17291 QW 17314 QW 17317 QW 17255 QW 17320 QW 16946 QW 16944 QW 16949 QW 16960 QW 17059 QW 16963 QW 17060 QW 17057 QW 17066 Part No: 7204614M Serial #s: QW 14735 QW 5709 QW 7623 QW 14560 QW 2701 QW 13306 QW 10665 QW 15180 QW 15114 QW 16358 QW 6058 QW 7968 QW 10807 Part No: 7204614S Serial #s: QW 12364 QW 15063 QW 18182 QW 17009 QW 18017 QW 18011 QW 6103 QW 14098 QW 18016 QW 17037 QW 11192 QW 18183 QW 17007 QW 16545 QW 14024 QW 16291 QW 9983 QW 17035 QW 12988 QW 17031 QW 18180 QW 15194 QW 11626 QW 17000 QW 15987 QW 16068 QW 16360 QW 18004 QW 15852 QW 16111 QW 16581 QW 11689 QW 15148 QW 18173 QW 13125 QW 17033 QW 15878 QW 15895 QW 17039 QW 18005 QW 17036 QW 10883 QW 10101 QW 14937 QW 12600 QW 18195 QW 17014 QW 12172 QW 13286 QW 14804 QW 15494 QW 16591 QW 18197 QW 12065 QW 17038 QW 11699 QW 15091 QW 13797 QW 15941 QW 18009 QW 6327 QW 12382 QW 16160 QW 13645 QW 14801 QW 16723 QW 17011 QW 18014 QW 15446 QW 17016 QW 13867 QW 13994 QW 9574 QW 15607 QW 15352 QW 16296 QW 13203 QW 14232 QW 11717 QW 14071 QW 15111 QW 18027
Smith And Nephew, Inc. Endoscopy Division is recalling Endocoupler , C-Mount 35 mm Focal Length Catalog Number: 7204614, 7204614M, 7204614S 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