CooperSurgical, Inc. LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Brand
CooperSurgical, Inc.
Lot Codes / Batch Numbers
Lot # 201809125 & 201809135
Products Sold
Lot # 201809125 & 201809135
CooperSurgical, Inc. is recalling LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures. due to Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where t. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Firm sent letter 8/19/2019. 1. Please discard the outer master 10- pack box containing barcode label . 2. Keep the individual seal pouches with correct expiration date. 3. Complete and return the acknowledgement and receipt form. 4. To return the product, Qurantine the affected product, complete and retun the acknowledegment and receipt form to CooperSurgical. If you have additional questions, please contact a CooperSurgical Product Surveillance representative at 203.601.5200 Ext. 3300 or email us at recall@coopersurgical.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026