Pharmedium Recalls Meperidine HCl Injections Due To Sterility Concerns
Pharmedium Services, LLC is recalling Meperidine HCl in 0.9% Sodium Chloride injections nationwide due to a lack of sterility assurance.
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 and involves a lack of sterility assurance in an injectable medication, which poses a significant risk of serious injury or hospitalization.
Plain-English summary
Pharmedium Services, LLC is voluntarily recalling Meperidine HCl in 0.9% Sodium Chloride in all strengths, doses, and packaging. The recall is being conducted because of a lack of sterility assurance for the product.
The affected product is distributed nationwide in the United States. The recall includes all lots of the medication that remain within their expiration dates. The source text does not specify the exact number of units affected or the specific dates of distribution.
Healthcare providers and patients should stop using the recalled product and contact their pharmacist or the recalling firm for further instructions. The source text does not report any specific illnesses or injuries associated with this recall.
The recalled product
- Product
- Meperidine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
- Manufacturer
- Pharmedium Services, LLC
- Category
- Drug — Injectable Medication
- 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 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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