FDA recall record

Humco Holding Group Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and recall — FDA D-1048-2014

Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia sp.

Class IIclassification
D-1048-2014official record ID
Feb 5, 2014report date

Recall record at a glance

Official recordD-1048-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHumco Holding Group, Inc.
Report dateFeb 5, 2014
Recall initiation dateNov 26, 2013
LocationTexarkana, TX, United States

Official product description

Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and relieves pain and itching of minor cuts, scrapes, burns and insect bites. Aqueous solution. Active Ingredients Benzalkonium chloride 0.13% - First Aid antiseptic, Lidocaine hydrochloride 2.5% - External analgesic. Sold under the following brands: a) Good Neighbor Pharmacy NDC 24385-593-46 , b) Quality Choice, NDC 63868-0488-02; c) Select Brand NDC 15127-885-59; d) Premier Value UPC 4098602556; e) Rite Aid Pharmacy UPC 011822576871; f) TopCare UPC 3680033436; g) Vida Mia UPC 847717060718; h) Humco 2 fl. oz NDC 0395-1637-92 i) Humco 3 fl. oz. NCD 0395-1637-93 ; 2 fl OZ (59 mL) and 3 FL OZ (90 mL) bottles, HUMCO, Texarkana, TX 75501.

Why the product was recalled

Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia sp.

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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