Pharmedium Recalls Rocuronium Bromide Due to Sterility Assurance Concerns
Pharmedium Services, LLC is recalling all Rocuronium Bromide products due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
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, which corresponds to a Severe rating under the rubric, particularly given the risk of infection associated with a lack of sterility assurance in a drug product.
Plain-English summary
Pharmedium Services, LLC is voluntarily recalling all Rocuronium Bromide products in all strengths, doses, and packaging. The recall is being conducted because of a lack of sterility assurance for the medication.
The affected products were distributed nationwide in the United States. The recall includes all lots of the medication that remain within their expiration dates.
Healthcare providers and consumers should stop using the recalled Rocuronium Bromide products and contact their pharmacist or healthcare provider for further instructions.
The recalled product
- Product
- Rocuronium Bromide in all strengths, all doses, and all packaging.
- Manufacturer
- Pharmedium Services, 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 remaining within expiry.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 42 recalled by Pharmedium Services, 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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