PlainRecalls
FDA Devices Moderate Class II Ongoing

Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.

Reported: July 30, 2025 Initiated: June 11, 2025 #Z-2137-2025

Product Description

Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.

Reason for Recall

The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.

Details

Recalling Firm
CooperSurgical, Inc.
Units Affected
475 units
Distribution
US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and Washington DC.
Location
Trumbull, CT

Frequently Asked Questions

What product was recalled?
Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.. Recalled by CooperSurgical, Inc.. Units affected: 475 units.
Why was this product recalled?
The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 30, 2025. Severity: Moderate. Recall number: Z-2137-2025.