The Recall Desk
SevereFDA (Drugs)·D-497-2015·Announced 2015-04-29

Attix Pharmaceuticals Recalls 5-Fluorouracil Due to Penicillin Cross-Contamination Risk

Attix Pharmaceuticals is recalling 5-Fluorouracil 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 classified this as an FDA Class II recall. Per the rubric, FDA Class II recalls involving significant injury risks or hospitalization reports are rated as Severe (4).

Plain-English summary

Attix Pharmaceuticals is recalling 5-Fluorouracil active pharmaceutical ingredient (API) packaged in bags or drums. The product was distributed nationwide to compounding pharmacies and research organizations.

The recall is being conducted because all lots repackaged and distributed between January 5, 2012, and February 12, 2015, were processed in a facility that also handled penicillin products. The facility lacked adequate separation between the products, creating a potential for cross-contamination with penicillin.

Compounding pharmacies and research organizations that received this product should stop using it and contact the recalling firm for instructions on return or disposal.

The recalled product

Product
5-Fluorouracil 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

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 →