Main Street Compounding Pharmacy Recalls Testosterone Vials Due to Adverse Reactions
Main Street Family Pharmacy is recalling 62 vials of Testosterone Cypionate/Propionate after receiving seven reports of skin abscesses.
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 adverse reactions (skin abscesses), which aligns with the rubric criteria for Severe severity involving significant injury reports or Class II classifications with adverse events.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling 62 vials of Testosterone Cypionate/Propionate 250mg/ml 10ml. The recall is being conducted by the U.S. Food and Drug Administration.
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. The source text does not explicitly state that the recalled testosterone product caused these specific abscesses, but the recall is associated with these reports.
The affected 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 codes distributed prior to and including 05/23/2013 are affected. Consumers should stop using the product and contact the pharmacy for further instructions.
The recalled product
- Product
- Testosterone Cypionate/Propionate 250mg/ml 10ml via, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Injectable
- Affected units
- 62
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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