FDA Device recall Z-2545-2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures
- FDA Device
- Class III
- terminated
- Published 2019-09-25
On 2019-09-25 the FDA classified a Class III recall of LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures by Coopersurgical, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2545-2019 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-08-19 |
| Published | 2019-09-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Coopersurgical |
| Distribution | US |
Product
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Reason
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.
Identifiers
| code_info | Lot # 201809125 & 201809135 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Coopersurgical
- INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set
FDA Device · Class I · 2026-09-30 · Coopersurgical - INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set
FDA Device · Class I · 2026-09-30 · Coopersurgical - Endosee System Convenience Kit with IV Tube
FDA Device · Class II · 2025-07-30 · Coopersurgical - Endosee System Convenience Kit
FDA Device · Class II · 2025-07-30 · Coopersurgical - HSG Procedure Tray
FDA Device · Class II · 2025-07-30 · Coopersurgical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2545-2019%22
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