Fertility Technology Resources, Inc. Tucker Embryo Catheter, Stylet, For use with Embryo Transfer Catheter, 23 CM, Sterile, Single Use Only, Order #: ft r 223, Manufactured by Fertility Technology Resources, Inc., Marietta, GA 30062 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Tucker Embryo Catheter, Stylet, For use with Embryo Transfer Catheter, 23 CM, Sterile, Single Use Only, Order #: ft r 223, Manufactured by Fertility Technology Resources, Inc., Marietta, GA 30062
Brand
Fertility Technology Resources, Inc.
Lot Codes / Batch Numbers
All units shipped before August 17, 2007
Products Sold
All units shipped before August 17, 2007
Fertility Technology Resources, Inc. is recalling Tucker Embryo Catheter, Stylet, For use with Embryo Transfer Catheter, 23 CM, Sterile, Single Use On due to Expiration Date for Sterility; The 5 year dating could not be validated/supported for sterility assurance.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Expiration Date for Sterility; The 5 year dating could not be validated/supported for sterility assurance.
Recommended Action
Per FDA guidance
All customers were contacted by telephone starting 9/13/2007. They were asked to return all Tucker family of catheters and all Morton IUI catheters that are on the shelves. A UPS call tag was sent to each customer to facilitate the return of the products. A follow up Urgent Device Recall letter was sent to all customers on 10/9/2007 reminding them to return all outstanding inventory when the UPS call tag arrives.
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
CA, CO, FL, GA, LA, ME, MD, MI, MS, NH, NJ, NY, NC, OH, TN, WA
Page updated: Jan 10, 2026