Main Street Family Pharmacy Recalls Compounded Methylprednisolone Vials
Main Street Family Pharmacy is recalling compounded methylprednisolone vials due to reports of skin abscesses.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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 constitute significant injury reports, meeting the criteria for a Severe rating.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling compounded preservative-free methylprednisolone 80mg/ml 10 ml vials. The recall was initiated after the firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to the product.
The source text does not specify the distribution scope, lot numbers, or specific dates for the recalled units. Consumers who have this product should contact their healthcare provider or the recalling firm for instructions on how to proceed.
The recalled product
- Product
- Lipo Blast w/o adenosine,Methionine 25mg, Inositol 50 mg, Choline 100mg, Methyl B-12 .25mg, B6 25mg, B5 12.5 mg, Lidocaine 10mg, B7 5mg, B1 12.5mg, B2 2.5mg, B3 12.5mg, Benzyl Alcohol .02ml 50ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059…
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Steroid
- Hazard
- Affected units
- 6
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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