Product description

Prescription medications

See a list of details to help identify the product.

Reason the product is recalled

The products have been supplied in containers without child-resistant closures. Please note that there is no concern regarding the quality or safety of this medicine other than the absence of child resistant packaging.

The hazards to consumers

If children gain access to the products there is the potential for inadvertent poisoning.

What consumers should do

Consumers are asked to consult their physician on an alternate treatment and then return the product to the place of purchase for a full refund.

Details to help identify the product.

Supplier running the recall

Pfizer Australia Pty Ltd

Who sold the product

Various Pharmacies nationwide

Identifying product features

HALCION (triazolam) & PONSTAN (mefenamic acid) & XANAX (alprazolam) - All Batches HALCION (triazolam) 0.125 mg tablets, Bottles of 50 AUST R number: 12304 PONSTAN (mefenamic acid) 250 mg capsules, Bottles of 50 AUST R number: 14387 XANAX (alprazolam) 2mg Tablets, Bottles of 50 AUST R number: 53931 (Discontinued December 2013)

Identifying numbers

Other identifying numbers

HALCION (triazolam) & PONSTAN (mefenamic acid) & XANAX (alprazolam) - All Batches

HALCION (triazolam) 0.125 mg tablets, Bottles of 50 AUST R number: 12304

PONSTAN (mefenamic acid) 250 mg capsules, Bottles of 50 AUST R number: 14387

XANAX (alprazolam) 2mg Tablets, Bottles of 50 AUST R number: 53931 (Discontinued December 2013)

Where the product was sold

Nationally

Responsible regulators

Regulators are established or appointed by government. They enforce regulations and rules.

Quote PRA number 2015/14593 when contacting a regulator about this recall.

Recall and remedy questions

Contact the Therapeutic Goods Administration if you have:

  • a question about the remedy being offered to you by the business that is responsible for managing this recall, or
  • concerns about the way the business is managing this recall.