Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
LHB Recalled by Lighthouse For The Blind Due to The product contains an iodine 10% Ampule (10%...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lighthouse For The Blind directly.
Affected Products
LHB, First Aid Type I Individual Kit, NSN: 6545-00-656-1092, antiseptics, Kit number: 2114002. First Aid Kit.
Quantity: 56,133 kits
Why Was This Recalled?
The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which is being recalled by the firm's distributor. The labeling of the iodine 10% Ampule labels state that the contents of the package are sterile and does not clarify that this sterility claim is only applicable to the applicator. The antiseptic solution that is applied to the skin is a cutaneous disinfectant, and is not sterili
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lighthouse For The Blind
Lighthouse For The Blind has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report