Reported Jul 24, 2024 · Ongoing

Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide…

Medical Depot Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medical Depot Inc. · 99 Seaview Blvd Fl 2 · Port Washington, NY · 11050-4606

Is this the product you have?

  • Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities
  • Model791BL (Blue)
Lot codes and dates
  • UPC822383019093 (791BL) All serial numbers beginning with 21S
Amount recalled
875 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.