Fellows "Mighty 8" Power strip — Class II medical device recall Z-0350-2018
Terminated recall by Merge Healthcare, Inc., reported 2018-01-24, distributed nationwide. Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8" Power Strip and TrippLite Power Stri
| Recall number | Z-0350-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merge Healthcare, Inc., Hartland, WI, United States |
| Recall initiated | 2017-04-06 |
| Classified | 2018-01-14 |
| Reported by FDA | 2018-01-24 |
| Terminated | 2019-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 1,150 power |
| Reason classes | device malfunction |
| Model numbers | 04175-0008, 13-00106-00 |
Product
Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite Power strip (PS-415-HGULTRA - Part Number 13-00106-00) are two components sold as part of the Merge Hemo System.
Reason for recall
Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8" Power Strip and TrippLite Power Strip due to overheat of input resistor causing the power strip to smoke.
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-0350-2018. 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.