RXQ Compounding Recalls Dexpantenol Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Dexpantenol 250mg/mL Injection Solution because the product lacks assurance of sterility.
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 agency classification is FDA Class II, and the hazard involves a lack of assurance of sterility in an injectable medication, which poses a significant risk of serious injury or infection.
Plain-English summary
RXQ Compounding LLC is voluntarily recalling Dexpantenol 250mg/mL (MDV) Injection Solution, 30mL per vial. The recall is being conducted because the product lacks assurance of sterility. The affected product is identified by NDC 70731-0932-30.
The recall covers all lots within the expiration date. The product was distributed nationwide in the United States. The source text does not specify the exact number of units recalled or the specific distribution dates.
Consumers and healthcare providers should stop using the recalled product and contact their pharmacist or healthcare provider for further instructions. No illnesses or injuries have been reported in the source text.
The recalled product
- Product
- DEXPANTHENOL 250MG/ML (MDV) INJECTION SOLN, 30ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0932-30
- Manufacturer
- RXQ Compounding LLC
- Category
- Drug — Injectable Medication
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 within expiry
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 86 recalled by RXQ Compounding 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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