Use cautionMedical device recall · FDA · Published June 14, 2024
Medical Depot Nitro Glide Knee Walker Recall: Risk of Falling
Medical Depot recalls Nitro Glide Knee Walker model 791BL (Blue) due to risk of falling if the tiller separates from the base. Affected units have serial numbers starting with 21S.
“Medical Depot Nitro Glide Knee Walker Recall: Risk of Falling.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54864-medical-depot-nitro-glide-knee-walker-recall-risk-of-falling. Based on FDA recall #Z-2354-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2354-2024%22&limit=1).
The FDA announced on June 14, 2024, that Medical Depot Inc. is recalling Nitro Glide Knee Walkers because the tiller can separate from the base, causing users to fall and sustain injuries. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Medical Depot
Product: Nitro Glide Knee Walker
Model: 791BL (Blue)
UPC: 822383019093
Serial numbers beginning with 21S
Quantity: 875 units
The hazard
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury.
Context
GovInfoNow's records show Medical Depot Inc. has one other recall on record since April 11, 2025, specifically the iGo2 DC Car Adapter Recall dated April 11, 2025, which cited a hot housing risk. Other recent recalls of similar products include the GE Medical Systems Giraffe OmniBed FRU Recall (May 1, 2026), the Arjo Tenor Patient Lift Recall (March 10, 2026), and the Community Products E-Pacer K660 recall (December 18, 2025).
How to tell if you have this one
Check for the Nitro Glide Knee Walker model 791BL (Blue) with serial numbers starting with 21S. The product was sold with UPC 822383019093.
Brand
Medical Depot
Product
Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Nationwide Foreign: Canada
Recall number
Product, codes & lots
Quantity
Z-2354-2024
Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities. Model: 791BL (Blue); UPC: 822383019093 (791BL) All serial numbers beginning with 21S
875 units
Z-2355-2024
Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities. Model: 791RD (Red); UPC: 822383019086 (791RD) All serial numbers beginning with 21S
667 units
Based on the official FDA remedy
What to do — step by step
Check for Separation
Look for if the tiller is loose or separated from the base and front caster assembly.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Nationwide Foreign: Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2354-2024 (June 14, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2354-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.