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McKesson 146-K320DDA-SFRecalls & reported problems

Mckesson Medical-Surgical Inc. · Lightweight Wheelchair, 20 Inches FLIP BACK DETACHABLE DESK ARMS | SWING-AWAY FOOTREST · 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 00612479223301), received between May 1, 2023 and May 1, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryMay 1, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

    (B)(6) HEALTHCARE WAS NOTIFIED OF A COMPLAINT INVOLVING A TRANSPORT WHEELCHAIR BY A PROVIDER, WHO STATED THAT THE PRODUCT "CAUSED SERIOUS INJURY TO USER." THERE WERE NO SPECIFIC DETAILS PROVIDED REGARDING HOW THE PRODUCT CAUSED THE INJURY, OR THE INJURY ITSELF. DRIVE IS ATTEMPTING TO CONTACT THE END USER DIRECTLY TO INVESTIGATE THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Insufficient Information

    MAUDE report 16844645 ↗

Other Wheelchair, Mechanical devices

All Wheelchair, Mechanical devices →

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