The Recall Desk
SevereFDA (Drugs)·D-959-2015·Announced 2015-04-29

Attix Pharmaceuticals Recalls Zolmitriptan Due to Penicillin Cross-Contamination Risk

Attix Pharmaceuticals is recalling zolmitriptan 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 recall is classified as FDA Class II. According to the rubric, an FDA Class II recall involving a significant hazard like penicillin cross-contamination (which can cause severe allergic reactions) maps to a severity score of 4 (Severe), especially given the lack of reported illnesses which prevents a higher score but the inherent risk prevents a lower one.

Plain-English summary

Attix Pharmaceuticals is recalling all lots of zolmitriptan active pharmaceutical ingredient (API) that were repackaged and distributed between January 5, 2012, and February 12, 2015. The product is packaged in varying grams or kilograms in bags or drums. The specific quantity mentioned in the structured data is 2,200 grams.

The recall was initiated because the zolmitriptan was repackaged in a facility that also handled penicillin products without adequate separation. This process created a potential for cross-contamination with penicillin. The affected product was distributed nationwide to compounding pharmacies and research organizations.

Consumers and healthcare professionals should check their inventory for zolmitriptan API from Attix Pharmaceuticals with distribution dates within the specified range. Those who have this product should stop using it and contact the recalling firm or their supplier for instructions on return or disposal.

The recalled product

Product
Zolmitriptan 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
Category
Drug — Active Pharmaceutical Ingredient
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 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.

See all 470 products in this recall →

Related recalls

Same manufacturer · Attix Pharmaceuticals

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Same hazard · penicillin cross contamination

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