Lighthouse For The Blind: Medical Device Recall in 2013 - (Recall #: Z-1091-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

LHB, Perishable Item Pack Type III. Kit number: 2114011-100. First Aid Kit.

Product Classification:

Class III

Date Initiated: March 22, 2013

Date Posted: April 17, 2013

Recall Number: Z-1091-2013

Event ID: 64776

Reason for Recall:

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

Status: Terminated

Product Quantity: 227 kits

Code Information:

All kits shipped between 1/12010 through 3/4/2013.

Distribution Pattern:

Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.

Voluntary or Mandated:

Voluntary: Firm initiated