LEEP Return Patient Pads — Class III medical device recall Z-2545-2019
Terminated recall by CooperSurgical, Inc., reported 2019-09-25, distributed nationwide. Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expi
| Recall number | Z-2545-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2019-08-19 |
| Classified | 2019-09-16 |
| Reported by FDA | 2019-09-25 |
| Terminated | 2020-07-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO, JP, MY |
| Quantity | 4,930 units |
| Reason classes | labeling |
| Lot numbers | 201809125, 201809135 |
| Model numbers | 6050PL |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2545-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.