Recall events
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Event 73918
Event summary
Timeline bucket February 17, 2016
Product types Device
Classifications Class II
Statuses Terminated
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
6 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 6
Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, adult, 8 pairs per case, 3) Aluminum crutch, youth, 1 pair per case, 4) Aluminum crutch 8 pairs per case, 5) Aluminum crutch, tall adult, 1 pair per case & 6) Aluminum crutch, tall adult, 8 pairs per case
Z-2101-2016
Recall number Z-2101-2016
Initiated February 17, 2016
Classification Class II
Status Terminated
Quantity 123,125 pairs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2101-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27128]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Code information Item #.: 1) 10400-1, 2) 10400-8, 3) 10401-1, 4) 10401-8, 5) 10402-1 & 6) 10402-8
Distribution pattern Nationwide Distribution
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[11153]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 6
EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ adjust aluminum crutch, tall adult, 1 pair per case & 6) EZ adjust aluminum crutch, tall adult, 8 pairs per case
Z-2102-2016
Recall number Z-2102-2016
Initiated February 17, 2016
Classification Class II
Status Terminated
Quantity 123,125 pairs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2102-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32388]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Code information Item #: 1) 10430-1, 2) 10430-8, 3) 10431-1, 4) 10431-8, 5) 10432-1 & 6) 10432-8
Distribution pattern Nationwide Distribution
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12607]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 6
Universal aluminum crutch, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Z-2103-2016
Recall number Z-2103-2016
Initiated February 17, 2016
Classification Class II
Status Terminated
Quantity 123,125 pairs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2103-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44289]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Code information Item #: RTL 10433
Distribution pattern Nationwide Distribution
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[10260]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 6
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Z-2104-2016
Recall number Z-2104-2016
Initiated February 17, 2016
Classification Class II
Status Terminated
Quantity 123,125 pairs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2104-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14492]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Code information Item #: 1) RTL 10400, 2) RTL 10402
Distribution pattern Nationwide Distribution
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[11171]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 6
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Z-2105-2016
Recall number Z-2105-2016
Initiated February 17, 2016
Classification Class II
Status Terminated
Quantity 123,125 pairs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2105-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[55994]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Code information Item #: 1) RTL 10400, 2) RTL 10402
Distribution pattern Nationwide Distribution
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8587]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 6
Direct Supply aluminum crutch, adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Z-2106-2016
Recall number Z-2106-2016
Initiated February 17, 2016
Classification Class II
Status Terminated
Quantity 123,125 pairs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2106-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44291]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Code information Item #: DS 10400
Distribution pattern Nationwide Distribution
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8593]
FDA event record
· Exact recall-number query on openFDA
