Main Street Compounding Pharmacy Recalls Methylprednisolone Vials Due to Skin Abscesses
Main Street Family Pharmacy is recalling compounded methylprednisolone vials after seven reports of skin abscesses. Consumers should stop using the product and contact their pharmacist.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves reports of skin abscesses, which constitutes significant injury reports under the severity rubric.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling Mic Ultra-Sulfur Free 10ml vials of compounded preservative-free methylprednisolone 80mg/ml. The recall was initiated after the firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to the product.
The affected units were distributed nationwide to specific states including 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. The recall covers all codes distributed prior to and including May 23, 2013.
Consumers who have this product should stop using it immediately and contact their pharmacist or the recalling firm at 888-658-6200 for instructions on how to return or dispose of the medication.
The recalled product
- Product
- Mic Ultra-Sulfur Free 10ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Steroid
- Hazard
- Affected units
- 1
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- all codes distributed prior to and including 05/23/2013
Distribution
Part of a larger recall action
This product is one of 299 recalled by Main Street Family Pharmacy, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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