Lighthouse For The Blind
Complete recall history across all FDA and CPSC categories — 8 total recalls
Lighthouse For The Blind 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 (8)
FDA medical device enforcement actions by Lighthouse For The Blind
| Date | Product | Reason | Class |
|---|---|---|---|
| Mar 22, 2013 | LHB, First Aid Type I Individual Kit, NSN: 6545-00-656-1092, antiseptics, Kit... | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, Perishable Item Pack Type III. Kit number: 2114011-100. First Aid Kit. | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, Perishable Items Pack Type IV. Kit number: 2114016-100. First Aid Kit. | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, Perishable Items Pack Type I , Kit Number: 2114002-100. First Aid ... | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povi... | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, First Aid Type IV Belt Type, NSN #6545-01-010-7754. Kit number: 114016... | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, Antiseptic Kit, Povidone Swab, Gauze Pads, and non-stick pads. Kit Numb... | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
| Mar 22, 2013 | LHB, First Aid Type III, NSN # 6545-00-656-1094, Kit number: 2114011. Fi... | The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is... | Class III |
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.
Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.
Explore More Recalls
Search recalls by category, state, reason, or firm across all our databases.