Medical Depot Inc.
Complete recall history across all FDA and CPSC categories — 9 total recalls
Medical Depot Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (9)
FDA medical device enforcement actions by Medical Depot Inc.
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 11, 2025 | iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Syste... | Potential for DC Power Supply housing to become hot to the touch and deform t... | Class I |
| Jun 14, 2024 | Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury ... | The tiller separates from the base/front caster assembly. If the knee walker ... | Class II |
| Jun 14, 2024 | Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury ... | The tiller separates from the base/front caster assembly. If the knee walker... | Class II |
| Feb 17, 2016 | EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum c... | Tip crutch failure involving the bottom of the metal portion which comes in c... | Class II |
| Feb 17, 2016 | Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair... | Tip crutch failure involving the bottom of the metal portion which comes in c... | Class II |
| Feb 17, 2016 | Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult,... | Tip crutch failure involving the bottom of the metal portion which comes in c... | Class II |
| Feb 17, 2016 | Universal aluminum crutch, 1 pair per case Aid the user in walking while r... | Tip crutch failure involving the bottom of the metal portion which comes in c... | Class II |
| Feb 17, 2016 | Direct Supply aluminum crutch, adult, 1 pair per case Aid the user in walk... | Tip crutch failure involving the bottom of the metal portion which comes in c... | Class II |
| Feb 17, 2016 | Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult,... | Tip crutch failure involving the bottom of the metal portion which comes in c... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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