The Recall Desk
SevereFDA (Drugs)·D-070-2014·Announced 2013-12-11

Main Street Compounding Pharmacy Recalls Depo-Testadiiol Due to Skin Abscess Reports

Main Street Compounding Pharmacy is recalling Depo-Testadiiol after seven reports of skin abscesses linked to compounded preservative-free 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 reports of skin abscesses, which constitutes significant injury reports, meeting the criteria for a Severe rating.

Plain-English summary

Main Street Family Pharmacy, LLC is recalling Depo-Testadiiol, a compounded medication, due to seven reports of adverse reactions in the form of skin abscesses. These reactions are potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials.

The recall covers 2 units of the product. The distribution pattern is nationwide, specifically 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. The recall includes all codes distributed prior to and including 05/23/2013.

Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions.

The recalled product

Product
Depo-Testadiiol, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
Affected units
2

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 →