Main Street Compounding Pharmacy Recalls Testosterone Pellets Due to Adverse Reactions
Main Street Family Pharmacy is recalling Testosterone Pellet 87.5mg units due to 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 agency classification is FDA Class II, and the source text reports specific adverse reactions (skin abscesses), which aligns with the rubric criteria for a Severe rating involving significant injury reports.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling 24 units of Testosterone Pellet 87.5mg. 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 codes were distributed prior to and including 05/23/2013.
The recall was initiated after the firm received seven reports of adverse reactions in the form of skin abscesses. The source text notes these reactions were potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials, although the specific product identified in the recall metadata is Testosterone Pellet 87.5mg.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Testosterone Pellet 87.5mg, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Prescription
- Affected units
- 24
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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