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Vive MOB1019BLKRecalls & reported problems

Vive Health LLC · Knee Walker (Black) · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00818323022896), received between Aug 5, 2026 and Aug 13, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Mechanical Problem” (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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 2 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Mechanical Problem1
  • Misassembled During Installation1

Patient problems

  • Bone Fracture(s)1
  • Laceration(s)1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 13, 2026Misassembled During Installation

    The customer reported that while using the mobility scooter, the seat rotated unexpectedly twice, causing her to fall in her garage. During the fall, she struck her ankle against brick steps. The customer reported sustaining an ankle fracture and a severe ankle sprain. She sought medical attention and reported that treatment included remaining non-weight-bearing for two weeks and the use of an ankle brace and walking boot for an estimated 4 to 12 weeks. The customer stated that, due to the pain following the incident, she immediately packaged and returned the product and did not take photographs. At the time of this report, the device has not been received for evaluation. Based on the information available, the customer's description of the event is not sufficiently clear to determine the cause of the reported incident. The customer reported that the seat rotated out of position twice; however, it could not be determined whether the seat was properly locked in place prior to use.

    Patient problems: Bone Fracture(s)

    MAUDE report 50234781 ↗
  • InjuryAug 5, 2026Mechanical Problem

    Customer reported a safety incident involving the All Terrain Knee Walker. While in use, the brake system failed, causing the customer to fall. There is a damaged/broken brake component as well as visible facial injury sustained from the fall.

    Patient problems: Laceration(s)

    MAUDE report 50141193 ↗

Other Walker, Mechanical devices

All Walker, Mechanical devices →

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