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Recall: MYNZEPLI 40 MG/ML SOLUTION FOR INJECTION IN A PRE-FILLED SYRINGE
Official notice
26 Oct 2026
Last checked
26 Oct 2026
An official AEMPS notice concerns Recall: MYNZEPLI 40 MG/ML SOLUTION FOR INJECTION IN A PRE-FILLED SYRINGE. A deviation has been detected in the syringe component that supports the fingers, which could cause it to loosen or detach during administration of the medicine Published 2026-10-26.
What to do now
Recall of all distributed units of the affected batch and return to the laboratory through the usual channels
Recall number
R_38/2026
Official notice
2026-10-26
The hazard
The hazard
A deviation has been detected in the syringe component that supports the fingers, which could cause it to loosen or detach during administration 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. Check the official notice for the affected products and next steps.
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Where it was sold
Where it was sold
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Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
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