LEEP Return Patient Pads recall
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Why was LEEP Return Patient Pads 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.
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
Lot # 201809125 & 201809135
- Product
- LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
- Recalling firm
- CooperSurgical, Inc.
- Quantity
- 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
- Recall date
- September 25, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)