The Recall Desk
SevereFDA (Drugs)·D-261-2014·Announced 2013-12-11

Main Street Compounding Pharmacy Recalls Pre-Menopausal Pack 3rd Month

Main Street Family Pharmacy is recalling Pre-Menopausal Pack 3rd Month units due to reports of skin abscesses potentially linked to compounded methylprednisolone.

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 rubric criteria for a Severe severity score.

Plain-English summary

Main Street Family Pharmacy, LLC is recalling 12 units of Pre-Menopausal Pack 3rd Month. The recall is being conducted because 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 affected products were distributed nationwide to the following states and districts: 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 includes all codes distributed prior to and including 05/23/2013.

Consumers who have purchased this product should stop using it and contact Main Street Family Pharmacy at 888-658-6200 for further instructions.

The recalled product

Product
Pre-Menopausal Pack 3rd Month, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
Affected units
12

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

Distributed nationwide across the United States.

The notice also names 39 states specifically:

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.

See all 299 products in this recall →