Medsolutions4U Multi-Function Electrodes to be used with… — Class II medical device recall Z-2565-2014
Terminated recall by Bio-Detek, Inc., reported 2014-09-10. Medsoultions4U Multi-Function Lifepak Electrodes, manufactured with an incorrect wire connector which could no
| Recall number | Z-2565-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bio-Detek, Inc., Pawtucket, RI, United States |
| Recall initiated | 2013-03-12 |
| Classified | 2014-09-02 |
| Reported by FDA | 2014-09-10 |
| Terminated | 2015-06-17 |
| Countries outside the US | DE, SI |
| Lot numbers | 0413 |
| Model numbers | 10C, 2033, 500 |
| Expiration dates | 2015-01-26 |
Product
Medsolutions4U Multi-Function Electrodes to be used with PhysioControl Lifepak Defibrillators, models 9, 10C, 11, 12, 15, 20, 500 and are indicated for Defibrillation, Cardioversion, Pacing, and Monitoring Part Number: 2033
Reason for recall
Medsoultions4U Multi-Function Lifepak Electrodes, manufactured with an incorrect wire connector which could not interface with the defibrillators
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-2565-2014. 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.