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