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Drive Devilbiss Healthcare · Model KA4285-2GWP · UDI-DI 00822383584164

ITJ
10
510(k) clearances
15,177
Adverse events (40 deaths)
29
Recalls
344
Facilities

Description

Seat Only for Nimbo, L, Wizard Purple

Recalls

DateFirmReason
2026-08-14Medline Industries, LPThe front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the f
2026-08-14Medline Industries, LPThe front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the f
2024-08-26Nova Ortho-Med IncFirm identified a potential risk for a fall hazard. When the end user is readjusting from the slouched seated position to an upright seated position, there is the potential for the
2024-08-26Nova Ortho-Med IncFirm identified a potential risk for a fall hazard. When the end user is readjusting from the slouched seated position to an upright seated position, there is the potential for the
2024-08-26Nova Ortho-Med IncFirm identified a potential risk for a fall hazard. When the end user is readjusting from the slouched seated position to an upright seated position, there is the potential for the
2024-06-14Medical Depot Inc.The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
2024-06-14Medical Depot Inc.The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
2023-09-13Breg IncDue to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
2023-06-15Invacare CorporationPremature failure of the seat during use, the plastic eyelets of the folding mechanism of the device's seat can break, and in a worst-case crossbar also breaks and the Rollator can
2022-01-10Compass Health Brands (Corporate Office)Wheel spoke may crack causing the wheel to separate from the axle may result in patient injuries, including bruising and lacerations requiring stitches.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.