Open official notice

Penethaject antibiotic injection

Official notice

17 May 2024

RecallScope risk estimate:CriticalAPVMA

An official APVMA notice concerns Penethaject antibiotic injection. Inability to withdraw the re-suspended product from the vial may lead to lower dosing and possible lack of efficacy. Published 2024-05-17.

What to do now

Do not use penethaject antibiotic injection from batch NZ45969 (powder) e101591 (cow 6 pack). Retailers and wholesalers should immediately quarantine all the stock on hand of the recalled product and contact elanco australia to arrange return and credit for the affected units. End users are advised to contact the retailer from which you purchased the product for replacement or refund.

Official notice

2024-05-17

The hazard

Inability to withdraw the re-suspended product from the vial may lead to lower dosing and possible lack of efficacy.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Check the official notice for the affected products and next steps.

Lots

NZ45969

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Where it was sold

Retailer information is not currently available in RecallScope. Check the official notice for distribution details.

Location 1

AU · Australia

Affected area 1

AU · Australia

Source & status

Source

Tier

official

Category

HOME

Recall details

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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