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No image published for this recall

Stemetil 5mg tablets

Official notice

1 Jun 2017

Last checked

1 Jun 2017

Low riskACCC

An official ACCC notice concerns Stemetil 5mg tablets. Affected packs may not contain the correct number of tablets. Published 2017-06-01.

What to do now

If you or someone you provide care for takes Stemetil 5mg tablets, please check the batch number (displayed on the packs and blister sheets) to see if it is affected by this recall. If you have a pack that has been affected by this issue, return any unused medicine to your pharmacy for a refund. If there are no anomalies with your product, you can choose to continue using it as normal. If you have any other questions or concerns about this issue, talk to your health professional or contact Sanofi-Aventis Medical Information on 1800 818 806.

Recall number

9d91262a-8171-4249-acc8-135fc77e6847

Official notice

2017-06-01

The hazard

Affected packs may not contain the correct number of tablets.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

16N0060

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Affected products

Product 1

Stemetil (prochlorperazine maleate) 5mg tablets AUST R 27564 Stemetil is used to treat nausea, vomiting and dizziness due to various causes, including migraine (severe headache). Batch number 16N0060 Expiry date 06/2018

Risk / hazard

Affected packs may not contain the correct number of tablets.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

AU · Australia

Affected area 1

AU · Australia

Source & status

Source

Tier

beta

Category

HOME

Classification

Pharmacy and medical products

App estimate

low

Recall details

Recall number

9d91262a-8171-4249-acc8-135fc77e6847

Classification

Pharmacy and medical products

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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