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Drive 13002SV-1Recalls & reported problems

Drive Devilbiss Healthcare · RespiratoryCarts/racks/cases/stands Product Description: Oxygen Cart, Silver Vein, Adj, 1/cs · Class 1

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383218403), received between Aug 17, 2020 and Aug 17, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Laceration(s)1

Recent adverse event reports

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

  • InjuryAug 17, 2020Fracture; Fracture

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS AN OXYGEN CART. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. THE WHEEL ON THE E-CYLINDER BROKE. THE CART FELL CAUSING A CUT ON THE PATIENT'S ANKLE. THE DEVICE IS 6 YEARS OLD.

    Patient problems: Laceration(s)

    MAUDE report 10418185 ↗

Other CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT) devices

All CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT) devices →

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