Lighthouse For The Blind recalls

Lighthouse For The Blind has 8 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 17 Apr 2013. The most frequent reason is sterility.

Total recalls8since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 17 Apr 2013

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 0 0%Class III 8 100%

Why lighthouse for the blind is recalled

Sterility8100%

Product types

Other Medical Devices8100%

By year

20138100%

All lighthouse for the blind recalls, newest first

8 total

Reported	Class	Recall	Company	Reason	Where
17 Apr 2013Device	CLASS III	LHB, First Aid Type I Individual Kit, NSN: 6545 recalled	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, Perishable recalled by Lighthouse For The Blind	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, Perishable Items Pack Type IV recalled by Lighthouse For The Blind	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, Perishable Items Pack Type I , Kit Number recalled	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg recalled	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, First Aid Type IV Belt Type, NSN #6545 recalled	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, Antiseptic Kit, Povidone Swab, Gauze Pads, and non-stick pads recalled	Lighthouse For The Blind	Sterility	Nationwide
17 Apr 2013Device	CLASS III	LHB, First Aid Type III, NSN # 6545-00-656-1094, Kit number recalled	Lighthouse For The Blind	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.