Reliable Drug Recalls Compounded All Midrin Products Due to Processing Controls
Reliable Drug is recalling compounded All Midrin products because of a lack of processing controls. The recall covers lots compounded between March 2015 and March 2016.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a lack of processing controls without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Reliable Drug/Reliable Compounding Pharmacy is recalling All Midrin (isometheptene mucate, dichloralphenazone and acetaminophen) products. These are prescription-only medications compounded by the pharmacy located in San Francisco, California.
The recall was initiated due to a lack of processing controls. The affected products include all lots compounded between March 24, 2015, and March 24, 2016, that are within their expiration dates.
The products were distributed in the United States, specifically in California, Hawaii, and New Mexico. Consumers and healthcare providers should stop using these products and contact their pharmacist or the recalling firm for further instructions.
The recalled product
- Product
- All Midrin (isometheptene mucate, dichloralphenazone and acetaminophen) Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.
- Manufacturer
- Reliable Rexall-A Compounding Pharmacy
- Category
- Drug — Compounded Prescription
- Hazard
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 lots compounded between 03/24/2015 and 03/24/2016 and within expiry.
Distribution
Part of a larger recall action
This product is one of 70 recalled by Reliable Rexall-A Compounding Pharmacy 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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