Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by CooperSurgical, Inc. Due to Discrepancy between the correct expiration dates on the...

Date: August 19, 2019
Company: CooperSurgical, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact CooperSurgical, Inc. directly.

Affected Products

LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.

Quantity: 4930 units

Why Was This Recalled?

Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About CooperSurgical, Inc.

CooperSurgical, Inc. has 83 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report