LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Reported: September 25, 2019 Initiated: August 19, 2019 #Z-2545-2019
Product Description
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
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.
Details
- Recalling Firm
- CooperSurgical, Inc.
- Units Affected
- 4930 units
- Distribution
- 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
- Location
- Trumbull, CT
Frequently Asked Questions
What product was recalled? ▼
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.. Recalled by CooperSurgical, Inc.. Units affected: 4930 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 25, 2019. Severity: Low. Recall number: Z-2545-2019.
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