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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94832

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 14, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Medical Depot Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

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)

Z-2354-2024
Recall number
Z-2354-2024
Initiated
June 14, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Medical Depot Inc.
Quantity
875 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

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

Code information

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

Distribution pattern

Nationwide Foreign: Canada

device · product 2 of 2

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)

Z-2355-2024
Recall number
Z-2355-2024
Initiated
June 14, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Medical Depot Inc.
Quantity
667 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

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

Code information

UPC: 822383019086 (791RD) All serial numbers beginning with 21S

Distribution pattern

Nationwide Foreign: Canada