DC power cable — Class II medical device recall Z-1586-2013
Terminated recall by Medrad Inc, reported 2013-07-03, distributed nationwide. The firm is recalling these power cables due to a latent design reliability issue and the potential for shorti
| Recall number | Z-1586-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medrad Inc, Indianola, PA, United States |
| Recall initiated | 2013-04-15 |
| Classified | 2013-06-24 |
| Reported by FDA | 2013-07-03 |
| Terminated | 2014-04-03 |
| Distributed | Nationwide (US) |
| Quantity | 1,066 |
| Model numbers | 3011992, 3011992W, 3011993, 3011993W, 3011994, 3011994W, 3011996, 3011996W, 3014268, 3014268W |
Product
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor, Physiological, Patient
Reason for recall
The firm is recalling these power cables due to a latent design reliability issue and the potential for shorting which can result in heating/melting of the cable jacket.
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-1586-2013. 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.