FDAClass IIJuly 24, 2024

Nitro Glide Knee Walker-offers users recovering from a recall

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

Why was Nitro Glide Knee Walker-offers users recovering from a recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UPC: 822383019093 (791BL) All serial numbers beginning with 21S

Product
Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities.…
Recalling firm
Medical Depot Inc.
Quantity
875 units
Distribution
Nationwide Foreign: Canada
Recall date
July 24, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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