Kanamycin Sulfate Recalled Due to Potential Penicillin Cross Contamination
Attix Pharmaceuticals is recalling Kanamycin Sulfate 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 that can cause severe reactions, meeting the criteria for a Severe rating.
Plain-English summary
Attix Pharmaceuticals is recalling Kanamycin Sulfate active pharmaceutical ingredient (API) packaged in bags or drums. The recall covers all lots of all products repackaged and distributed between January 5, 2012, and February 12, 2015.
The recall was initiated because the products were repackaged in a facility that also handled penicillin products without adequate separation. This condition creates the potential for cross-contamination with penicillin. The affected quantity is 34,765 grams.
The product was distributed nationwide to compounding pharmacies and research organizations. Consumers and healthcare providers should stop using the affected Kanamycin Sulfate API and contact their supplier or the recalling firm for instructions on return or disposal.
The recalled product
- Product
- Kanamycin Sulfate 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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