CooperSurgical, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2545-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class III

Date Initiated: August 19, 2019

Date Posted: September 25, 2019

Recall Number: Z-2545-2019

Event ID: 83704

Reason for Recall:

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.

Status: Terminated

Product Quantity: 4930 units

Code Information:

Lot # 201809125 & 201809135

Distribution Pattern:

USA: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, & WV. Distribution US nationwide, Canada, Colombia, Japan, & Malaysia

Voluntary or Mandated:

Voluntary: Firm initiated