Strides Pharma Inc. has recalled 1,032 bottles of Prednisone (prednisone) 20 mg Tablets because a 2.5 mg tablet was discovered inside a bottle intended to contain only 20 mg tablets. This recall involves 100-count bottles of the prescription medication distributed nationwide to pharmacies. No incidents or injuries have been reported to date regarding this mix-up.
A patient who unintentionally takes a 2.5 mg tablet instead of their prescribed 20 mg dose would receive significantly less medication than required. This dosage error could lead to the underlying condition not being properly treated, potentially resulting in a return or worsening of symptoms.
You have 2 options:
Quantity: 1032 bottles. Manufactured by Strides Pharma Science Ltd. in India.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.