Main Street Compounding Pharmacy Recalls B-12 Mixture Due to Adverse Reactions
Main Street Family Pharmacy is recalling 196 units of B-12 mixture after seven reports of skin abscesses linked to a related compounded product.
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 reported adverse reactions (skin abscesses), which aligns with the 'Severe' criteria for significant injury reports or Class II recalls with hospitalization/injury potential.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling 196 units of B-12 mixture. The product was 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. All units distributed prior to and including May 23, 2013, are affected.
The recall was initiated after the firm received seven reports of adverse reactions in the form of skin abscesses. These reactions were potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials, which are related to the recalled B-12 mixture.
Consumers who have this product should stop using it and contact Main Street Family Pharmacy at 888-658-6200 for instructions on how to return the product.
The recalled product
- Product
- B-12 mixture, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Medication
- Affected units
- 196
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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