Ethicon, Inc. US Gynecare PROLIFT Total Pelvic Repair System PFRT01 Ethicon Deutschland Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Gynecare PROLIFT Total Pelvic Repair System PFRT01 Ethicon Deutschland
Brand
Ethicon, Inc. US
Lot Codes / Batch Numbers
Product Code PFRT01 Lot Number 2990052 2007-12
Products Sold
Product Code PFRT01 Lot Number 2990052 2007-12
Ethicon, Inc. US is recalling Gynecare PROLIFT Total Pelvic Repair System PFRT01 Ethicon Deutschland due to The pre-printed outer box incorrectly identifies the product as GYNECARE PROLIFT Total Pelvic Floor System (Product Code PFRT01). The contents of the. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The pre-printed outer box incorrectly identifies the product as GYNECARE PROLIFT Total Pelvic Floor System (Product Code PFRT01). The contents of the box actually contain GYNECARE PROLIFT Anterior Pelvic Floor System (Product Code PFRA01)
Recommended Action
Per FDA guidance
Recall notifications were sent by 2nd day air UPS delivery on April 20, 2007 to all hospitals Director of Surgery, OR Managers and Materials Managers.
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 noticePage updated: Jan 10, 2026