Quickie 2 Quickie 2, Quickie 2 Lite, Quickie 2 Lite 2.0Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00016958043815), received between Sep 20, 2021 and Sep 25, 2024 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).

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 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 25, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE DEALER REPORTED THAT THE LEFT-SIDE WHEEL LOCK IS NO LONGER LOCKING AND FELL APART UNDER NORMAL USE. THE DEALER DID NOT REPORT ANY INJURIES OR ADVERSE IMPACT TO THE END USER, AND THE DEALER REQUESTED A WARRANTY REPLACEMENT OF THE LEFT-SIDE WHEEL LOCK ASSEMBLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20302306 ↗
• MalfunctionSep 25, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  ACCORDING TO THE DEALER, THE WHEELCHAIR'S LEFT-SIDE WHEEL LOCK BECAME LOOSE; THIS OCCURRED WHILE THE END-USER USED THE CHAIR ON (B)(6) 2024.THE DEALER REPORTED THE TECHNICIAN WENT TO THE END USER'S HOME TO TIGHTEN THE WHEEL LOCK THREE (3) SEPARATE TIMES, BUT THE LEFT-SIDE WHEEL LOCK WILL NO LONGER REMAINED TIGHTENED. THE DEALER DID NOT REPORT ANY INJURIES OR ADVERSE IMPACT TO THE END USER, AND THE DEALER REQUESTED A WARRANTY REPLACEMENT OF THE LEFT-SIDE WHEEL LOCK ASSEMBLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20301708 ↗
• InjurySep 20, 2021Human-Device Interface Problem; Mechanics Altered; Unintended Movement; Misassembly by Users; Insufficient Device Problem Information; Misassembled During Installation; Misassembly During Maintenance/Repair; Human-Device Interface Problem; Mechanics Altered; Unintended Movement; Misassembly by Users; Insufficient Device Problem Information; Misassembled During Installation; Misassembly During Maintenance/Repair

  PLEASE SEE INITIAL MDR 9616084-2021-00055; THIS REPORT IS BEING FILED AS PER 21 CFR PART 803.56. ADDITIONAL INFORMATION WAS IDENTIFIED DURING THE LEGAL CASE, REGARDING THE INCIDENT WHERE THE USER FELL AT HER HOME TRANSFERRING FROM THE TOILET BACK TO HER CHAIR. THE ER DIAGNOSIS FROM THE INCIDENT INCLUDED: SYNCOPE AND COLLAPSE; FALL ON SAME LEVEL, UNSPECIFIED; FRACTURE OF SHAFT OF FEMUR - DISTAL SHAFT RIGHT AND DISTAL LEFT; PAIN IN LEFT HIP; PAIN IN RIGHT HIP; ABNORMAL ELECTROCARDIOGRAM [ECG][EKG]; ALCOHOL USE, UNSPECIFIED WITH INTOXICATION; ESSENTIAL (PRIMARY) HYPERTENSION; HYPOKALEMIA. BLOOD ALCOHOL CONTENT WAS MEASURED AT 192.0 MG/DL, WHICH WAS CONFIRMED AS HIGH AND HER AST WAS CONSISTENT WITH ALCOHOL ABUSE, ACCORDING TO THE ER DOCTOR. THE ACCOUNT OF THE EVENT FROM THE ER WAS THAT THE DETAILS WERE HAZY TO HER. SHE WAS CONFUSED AT THE TIME AND WHEN SHE "CAME TO" SHE CALLED HER DAUGHTER'S CELL PHONE BUT WAS STILL DISORIENTED. SHE DID NOT KNOW WHAT HAD HAPPENED AND WHERE SHE WAS. MEDICAL RECORDS ALSO DOCUMENTED THAT SHE DID LOSE CONSCIOUSNESS.

  Patient problems: Confusion/ Disorientation; Fall; High Blood Pressure/ Hypertension; Hypokalemia; Limb Fracture; Nervous System Injury; Non specific EKG/ECG Changes; Pain; Syncope/Fainting; Unspecified Musculoskeletal problem

  MAUDE report 12499227 ↗