MediTrace Cadence Adult Zoll — Class II medical device recall Z-2546-2015
Terminated recall by Covidien LLC, reported 2015-09-09, distributed nationwide. Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result
| Recall number | Z-2546-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, North Haven, CT, United States |
| Recall initiated | 2015-08-19 |
| Classified | 2015-09-02 |
| Reported by FDA | 2015-09-09 |
| Terminated | 2017-05-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, DK, NZ |
| Quantity | 114,000 sets |
| Lot numbers | 513426X, 516313X, 519124X |
| Model numbers | 22770PC |
Product
MediTrace Cadence Adult Zoll, Preconnect Defibrillation Electrode, Nonsterile Item Code:22770PC
Reason for recall
Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result in a potentially increased risk for reduced or no patient therapy and patient and/or clinician burns
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-2546-2015. 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.