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Modpod 12.1000Recalls & reported problems

Hollywog, LLC · Modpod brand powered, static/intermittent, mobile traction system · Class 2

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 00853096004151), received between Nov 9, 2017 and Nov 9, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operational Issue” (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

  • Device Operational Issue1
  • Protective Measures Problem1

Patient problems

  • No Known Impact Or Consequence 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 9, 2017Device Operational Issue; Protective Measures Problem; Device Operational Issue; Protective Measures Problem

    THE DEVICE HAS FULL SCREEN FUNCTIONALITY, BUT WILL NOT PULL AT ALL. HE AND HIS CA HAS TRIED TURNING OFF AND ON THE DEVICE. WHEN ASKED TO CALIBRATE HIS DEVICE, IT WILL NOT BRING HIM TO THE SCREEN TO CALIBRATE. ALSO, THE PATIENT SWITCH WOULD NOT END TREATMENT PREVIOUSLY, SO THE CA IS SENDING BACK THE PATIENT SWITCH.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7014825 ↗

Other Equipment, Traction, Powered devices

All Equipment, Traction, Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.