Losartan Potassium Recalled for Potential Penicillin Cross Contamination
Attix Pharmaceuticals is recalling Losartan Potassium active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.
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 potential cross-contamination with penicillin, a high-risk allergen, which aligns with the 'Severe' criteria for significant injury risk or high-risk pathogens/allergens.
Plain-English summary
Attix Pharmaceuticals is recalling all lots of Losartan Potassium active pharmaceutical ingredient (API) that were repackaged and distributed between January 5, 2012, and February 12, 2015. The product was packaged in varying grams or kilograms in bags or drums. The total quantity involved is 6,525 grams.
The recall is being conducted because the API was repackaged in a facility that also handled penicillin products without adequate separation. This process created a potential for cross-contamination with penicillin. The product was distributed nationwide to compounding pharmacies and research organizations.
No specific illnesses or injuries have been reported in the source text. Compounding pharmacies and research organizations that received this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Losartan Potassium active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
- Manufacturer
- Attix Pharmaceuticals
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 repackaged and distributed between 01/05/12 to 02/12/15
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 470 recalled by Attix Pharmaceuticals 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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