Urologix, Inc. Urologix Microwave Delivery System 3.0 - 5.0. For use with prostatic urethra lengths of 3.0-5.0 cm only. Model TA1121D. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Urologix Microwave Delivery System 3.0 - 5.0. For use with prostatic urethra lengths of 3.0-5.0 cm only. Model TA1121D.
Brand
Urologix, Inc.
Lot Codes / Batch Numbers
Individual Catheter lot numbers: M002671, M002672, M002589 and M002736 for model TA1121D. Kit box lot numbers: KP011206, KP053006B, KP053006C, KP060205, KP0011206.
Products Sold
Individual Catheter lot numbers: M002671,M002672, M002589 and M002736 for model TA1121D. Kit box lot numbers: KP011206, KP053006B, KP053006C, KP060205, KP0011206.
Urologix, Inc. is recalling Urologix Microwave Delivery System 3.0 - 5.0. For use with prostatic urethra lengths of 3.0-5.0 cm due to The catheter in the kit matches the description on the kit and pouch label; however, an incorrect label was placed onto the catheter during manufactur. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The catheter in the kit matches the description on the kit and pouch label; however, an incorrect label was placed onto the catheter during manufacturing.
Recommended Action
Per FDA guidance
A letter dated 3/16/07 was FedEx overnight to consignees. The letter described the product, problem and gave instructions for returning and replacing the affected product.
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