Main Street Compounding Pharmacy Recalls Medroxyprogesterone Due to Adverse Reactions
Main Street Family Pharmacy is recalling 4 units of Medroxyprogesterone 150mg due to reports of skin abscesses linked to a related 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 agency classification is FDA Class II, and the source text reports adverse reactions (skin abscesses), which aligns with the rubric criteria for Severe severity involving Class II recalls with injury reports.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling four units of Medroxyprogesterone 150mg w/lid, 1ml. 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.
The affected units were distributed nationwide, specifically to 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 included in this recall.
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm at 888-658-6200 for further instructions.
The recalled product
- Product
- Medroxyprogesterone 150mg w/lid, 1ml 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
- 4
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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