Manufacturer
37 recalls in our database name Invacare Corporation as the manufacturing or recalling firm.
Of the 37 recalls from Invacare Corporation we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (49%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Invacare is recalling Dianz Capacitors used in PerfectO2 Oxygen Concentrators because they may rupture and cause a fire.
Invacare is recalling 5,963 Perfecto 2 V Oxygen Concentrators because defective sieve beds allow dust to migrate, reducing oxygen concentration.
Invacare is recalling 819 M41 powered wheelchair controllers that may cause momentary loss of control due to non-standard factory programming.
Invacare is recalling 465 Aquatec Fixed Backrests because they may detach from the frame under uneven load, posing a risk of injury.
Invacare is recalling 227 Tracer IV wheelchairs in Michigan because the wheels were warped and wobbled when rolled.
Invacare is recalling Aquatec Ocean mobile shower and toilet commodes because backrest cushion fixtures may unlatch in reclined or tilted positions.
Invacare is recalling power wheelchairs with specific joysticks due to unintended slowing or acceleration. Users should stop using the device and contact Invacare.
Invacare is recalling 285 CHAMPION Medical Recliners because the seat pad may reach elevated temperatures and the cord set labeling is incorrect.
Invacare is recalling three Solara 3G custom manual wheelchairs because the wheels may rotate freely despite the hub brake being engaged.
Invacare is recalling height adjustable walking canes because the height-lock button may compress unexpectedly, causing the cane to collapse and potentially injure the user.
Invacare is voluntarily recalling 21,168 I-Fit Shower Chairs (Models 9780, 9781, 9781-1) based on returned units and adverse event reports.
Invacare is recalling specific TDX power wheelchairs because a defect in the post fuse assembly could cause a short circuit, leading to fire and serious injury.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
Invacare
American medical equipment manufacturer
Source: Wikidata (Q4994426), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.