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RENASYS GO 66020914Recalls & reported problems

Smith & Nephew Medical Limited · RENASYS GO 300ml Canister with Solidifier · Class 2

Data updated Oct 13, 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 00040565127323), received between Jun 24, 2021 and Jun 24, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “False Alarm” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • False Alarm1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJun 24, 2021False Alarm; False Alarm

    IT WAS REPORTED THAT, DURING NPWT WITH RENASYS GO, THE 300ML CANISTER IS CAUSING THE PUMP TO DISPLAY "FULL ALARM" EVEN THOUGH THE CANISTER IS EMPTY. THE CANISTER IS EXCHANGED TO SOLVE THE PROBLEM. PATIENT HAS NOT BEEN HARMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12058124 ↗

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Sources and updates

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