FDA Recall
Terminated
Endocoupler, C-Mount 30 mm Focal Length Catalog Number: 7204823, 7204823S
Recall: Z-0704-04
·
Initiated February 19, 2004
Recall
- Recall Number
- Z-0704-04
- Event Number
- 28423
- Firm
- Smith And Nephew, Inc. Endoscopy Division
- FEI Number
- 3003604053
- Product Code
- FXM
- Status
- Terminated
- Root Cause
- Other
- Initiated
- February 19, 2004
- Posted
- July 20, 2004
- Terminated
- June 28, 2006
- Address
- 150 Minuteman Rd, Andover, MA, 01810-1031
Description
Endocoupler, C-Mount 30 mm Focal Length Catalog Number: 7204823, 7204823S
Reason
Endocouplers assembled with screws that cannot be effectively sterilized
Action
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.
Distribution
AL, AZ, CA, CT, PA, MA, ME, MI, MO, NC, NH, NJ, NY, OH, UT , TN, TX, VT, WA Foreiing:Australia, Canada, China, Brazil, France, Germany, Greece, India, Italy, Japan.Korea, Netherlands, Norway, Portugal, South Africa, Spain, Turkey, UK
Quantity
28 units