Medical Supply Liquidators Recalls Unapproved MIC Injection Vials
Medical Supply Liquidators LLC is recalling MIC Injection USP vials because the manufacturer is not registered with the FDA and the product lacks an approved NDA/ANDA.
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, but the source text does not report any illnesses or injuries, and the hazard is primarily regulatory (unapproved/unregistered manufacturer) rather than a specific physical contamination or defect causing harm.
Plain-English summary
Medical Supply Liquidators LLC is recalling MIC Injection USP, sterile, 10 ml and 30 ml vials intended for intramuscular or deep subcutaneous use. The product was manufactured by CB Inc. for Sunshine Labs. The recall is being conducted because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA), and the manufacturing firm is not registered with the FDA as a drug manufacturer.
The recall covers all lot numbers and expiration dates. The product was distributed nationwide and to Canada, the United Kingdom, Australia, Slovenia, Germany, Spain, Finland, and Croatia. The source text does not specify the number of units recalled or report any illnesses or injuries associated with the product.
Consumers and healthcare providers should stop using the recalled product and contact Medical Supply Liquidators LLC or their supplier for further instructions on return or disposal.
The recalled product
- Product
- MIC Injection USP, Sterile, 10 ml vial and 30 ml vial, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us
- Manufacturer
- Medical Supply Liquidators Llc
- Category
- Drug — Injectable
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 lot numbers and exp dates
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 15 recalled by Medical Supply Liquidators 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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