LHB, Perishable recall: Sterility Concern
LHB, Perishable Items Pack Type IV. Kit number: 2114016-100. First Aid Kit.
Why was LHB, Perishable 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
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All kits shipped between 1/12010 through 3/4/2013.
- Product
- LHB, Perishable Items Pack Type IV. Kit number: 2114016-100. First Aid Kit.
- Recalling firm
- Lighthouse For The Blind
- Quantity
- 425 kits
- Distribution
- 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.
- Recall date
- April 17, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)