Severity
Moderate
FDA Drug recall · Reported February 5, 2014
Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia sp.
Humco Holding Group, Inc recalled Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and relieves pain an… - a moderate-severity action.
Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and relieves pain an… was recalled by Humco Holding Group, Inc in February 5, 2014. Reason: Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia…. Check the official notice for the remedy. Verify recall #D-1048-2014 with the FDA Drug before acting.
The recall
Humco Holding Group, Inc issued this moderate-severity FDA Drug recall-Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia….
Sourced from official FDA Drug enforcement records. Verify recall #D-1048-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1048-2014) was formally reported on February 5, 2014, with the manufacturer initiating the action on November 26, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Humco Holding Group, Inc is listed as the recalling firm, operating out of Texarkana, TX. The number of affected units is not disclosed in the agency filing, which is common for drug and food recalls where lot-level tracking supersedes unit counts.
The documented reason for this recall is: Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia sp. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
Unknown
Related Recalls
6
5 from same agency
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.
Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia sp.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1048-2014 |
| Date reported | February 5, 2014 |
| Date initiated | November 26, 2013 |
| Recalling firm | Humco Holding Group, Inc |
| Firm location | Texarkana, TX |
| Affected scope | Not disclosed |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported February 5, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.