Main Street Compounding Pharmacy Recalls L-Arginine Due to Adverse Reaction Reports
Main Street Compounding Pharmacy is recalling L-Arginine 100mg/ml 30ml vials after receiving seven reports of skin abscesses potentially linked to the 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 recall is classified as FDA Class II and involves reported adverse reactions (skin abscesses), which aligns with the rubric criteria for Severe severity involving significant injury reports or Class II classifications with hospitalization/injury potential.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling 23 units of L-Arginine 100mg/ml 30ml vials. The recall is being conducted by the U.S. Food and Drug Administration under recall number D-154-2014.
The firm initiated the recall after receiving 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 source text does not specify the exact mechanism of the link or if the L-Arginine product itself was contaminated, but the recall is associated with these reported adverse events.
The affected units 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. All codes distributed prior to and including 05/23/2013 are included in this recall. Consumers should contact the recalling firm at 888-658-6200 for further instructions.
The recalled product
- Product
- L-Arginine 100mg/ml 30ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Medication
- Affected units
- 23
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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