The Recall Desk
SevereFDA (Drugs)·D-953-2015·Announced 2015-04-29

Attix Pharmaceuticals Recalls Vidarbine Monophosphate Due to Penicillin Cross-Contamination Risk

Attix Pharmaceuticals is recalling Vidarbine Monophosphate active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

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: FDA Class II recall involving a high-risk allergen (penicillin) cross-contamination in a pharmaceutical ingredient, which poses a significant risk of severe allergic reactions or anaphylaxis to sensitive individuals, meeting the criteria for Severe severity.

Plain-English summary

Attix Pharmaceuticals is recalling all lots of Vidarbine Monophosphate 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 recall is being conducted because the API was repackaged in a facility that also handled penicillin products without adequate separation, creating a potential for cross-contamination with penicillin.

The affected product was distributed nationwide to compounding pharmacies and research organizations. No specific illness or injury reports are mentioned in the source text, but the presence of penicillin contamination poses a significant risk to individuals with penicillin allergies.

Compounding pharmacies and research organizations that received this product should stop using it immediately and contact Attix Pharmaceuticals for instructions on return or disposal. Consumers should not use any Vidarbine Monophosphate API from this source and should consult their healthcare provider if they have concerns about potential exposure.

The recalled product

Product
Vidarbine Monophosphate 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 →

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Same hazard · allergen penicillin

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