Severity
Moderate
FDA Drug recall · Reported December 11, 2013
The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials.
Main Street Family Pharmacy, LLC recalled Mic 30ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-… - a moderate-severity action.
Mic 30ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-… was recalled by Main Street Family Pharmacy, LLC in December 11, 2013. Reason: The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to comp…. Check the official notice for the remedy. Verify recall #D-230-2014 with the FDA Drug before acting.
The recall
Main Street Family Pharmacy, LLC issued this moderate-severity FDA Drug recall-The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to comp….
Sourced from official FDA Drug enforcement records. Verify recall #D-230-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-230-2014) was formally reported on December 11, 2013, with the manufacturer initiating the action on May 28, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Main Street Family Pharmacy, LLC is listed as the recalling firm, operating out of Newbern, TN. Federal records list the affected scope as 16 units.
The documented reason for this recall is: The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials. Distribution data in the federal record shows the product reached: nationwide, specifically: AK, AL, AZ, CA, CO, CT, DC, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WV. 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, 3 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 - 1,360 cosmetics & personal care 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
16 units
Related Recalls
6
3 from same agency
Mic 30ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-230-2014 |
| Date reported | December 11, 2013 |
| Date initiated | May 28, 2013 |
| Recalling firm | Main Street Family Pharmacy, LLC |
| Firm location | Newbern, TN |
| Affected scope | 16 units |
| Distribution | nationwide, specifically: AK, AL, AZ, CA, CO, CT, DC, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WV |
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 December 11, 2013. 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.