FDAClass IIJuly 30, 2025

Endosee System Convenience Kit recall: Sterility Concern

Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System Convenience Kit

Why was Endosee System Convenience Kit 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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model Number: ES-TRAY. UDI-DI: 60888937027268. Lot Numbers: 335995, 339340, 339341, 339342, 339343, 339344, 339345, 343008.

Product
Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System Convenience Kit
Recalling firm
CooperSurgical, Inc.
Quantity
991 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.
Recall date
July 30, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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