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Jurnista Hydromorphone Hydrochloride 8 mg Prolonged Release Tablet Blister Pack
Official notice
20 Feb 2019
Last checked
20 Feb 2019
An official ACCC notice concerns Jurnista Hydromorphone Hydrochloride 8 mg Prolonged Release Tablet Blister Pack. Damage to the outer coating of the tablets may affect the release rate or dosage of the medicine. Published 2019-02-20.
What to do now
Check your Jurnista packaging to see if you have any tablets from batch number IALS400. If so, check the blister packs and tablets for any signs of damage (do not remove tablets from the packaging unless they are going to be consumed straight away). If the blister pack or tablets are damaged do not consume them. Return the entire Jurnista box to your dispensing pharmacy to discuss replacement options. In the likely event that the blister pack and tablets are not damaged, you should continue to take the medication as prescribed by your doctor. If you have any questions or concerns about this issue, talk to your doctor or pharmacist. You may also contact Janssen's Medical Information Department on 1800 226 334 or email medinfo@janau.jnj.com
Recall number
09738ca9-21a9-4e55-b5b3-c0806fb0d31e
Official notice
2019-02-20
The hazard
The hazard
Damage to the outer coating of the tablets may affect the release rate or dosage of the medicine.
How to check if you're affected
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.
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Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
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Source & status
Source & status
Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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