PadPro — Class II medical device recall Z-1317-2013
Terminated recall by ConMed Corporation, reported 2013-05-22, distributed nationwide. ConMed was notified by the contract manufacturer that their wire/connector supplier reported damage to the con
| Recall number | Z-1317-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ConMed Corporation, Utica, NY, United States |
| Recall initiated | 2013-05-03 |
| Classified | 2013-05-13 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2015-08-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | SA |
| Lot numbers | Y011013-13, Y012513-02, Y020713-05, Y021413-03, Y030113-04, Y092012-21, Y102612-12, Y110912-20, Y112912-10, Y121312-19 |
| Model numbers | 2001M-C |
Product
PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C. The PadPro(R) Adult Radiotransparent Multifunction Electrodes with Carbon Leadwires and Medtronic(R) Connector are intended to be used in external pacing, defibrillation and monitoring applications
Reason for recall
ConMed was notified by the contract manufacturer that their wire/connector supplier reported damage to the connector tooling which could pinch or compress the lead wire filaments and potentially render the device incapable of delivering the appropriate energy or shock to the patient and/or could cause potential injury to user or patient.
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-1317-2013. 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.