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RENASYS GO 66800603Recalls & reported problems

Smith & Nephew Medical Limited · RENASYS GO O-Ring · Class 2

All models of RENASYS GO (3)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00040565125299), received between Nov 10, 2020 and Nov 10, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Charge” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Failure to Charge1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 10, 2020Failure to Charge; Failure to Charge

    IT WAS REPORTED THAT THE RENASYS IS NOT CHARGING. NO INJURY TO PATIENT REPORTED DUE THIS EVENT. UNKNOWN HOW THE TREATMENT WAS FINISHED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10819804 ↗

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Sources and updates

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