CLASS II ONGOING Device recall · Reported 24 Jul 2024 · FDA Enforcement Report
Nitro Glide Knee Walker-offers users recovering recalled
Medical Depot is recalling Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability, distributed nationwide in the US. The recall was initiated on 14 Jun 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2355-2024
- FDA event ID
- 94832
- Recalling firm
- Medical Depot, Port Washington, NY
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 14 Jun 2024
- FDA classified
- 12 Jul 2024
- Reported
- 24 Jul 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Hip & Knee Implants
Timeline
| 14 Jun 2024 | Recall initiated by company | |
| 12 Jul 2024 | Classified by FDA | +28 days |
| 24 Jul 2024 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Product as listed by the FDA
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)
Where it was distributed
Nationwide Foreign: Canada
Questions about this recall
Why was it recalled?
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Which lots are affected?
UPC: 822383019086 (791RD) All serial numbers beginning with 21S
Where was it sold?
Nationwide Foreign: Canada
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 94832This product is part of a recall event; the main page for the event is Nitro Glide Knee Walker-offers users recovering recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Nitro Glide Knee Walker-offers users recovering recalled | Medical Depot | Other | Nationwide |
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|---|---|---|---|---|---|
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|---|---|---|---|---|---|
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| Device | CLASS II | U2 Total Knee System Femoral offset bushing recalled | United Orthopedic | Device Malfunction | Nationwide |