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CooperSurgical, Inc. recalls LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Recalled September 25, 2019 · FDA recall Z-2545-2019 · CooperSurgical
Hazard
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. · FDA Class III
Units
4930 units
Sold at
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
Description
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.
Product
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Manufacturer(s)
CooperSurgical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →