FDA Recalls Lupin Steroid Eye Drops Over Contamination

More than 2.5 million bottles of a prescription eye medication are being recalled across the United States. The Food and Drug Administration (FDA) raised concerns after finding foreign material in some bottles.

Lupin Pharmaceuticals Inc. recalled 2,530,182 bottles of prednisolone acetate ophthalmic suspension, a type of eye drop. This suspension treats inflammation after eye surgery and helps with certain eye injuries. The bottles were made in Pithampur, India, and sold in different sizes: 5 mL, 10 mL, and 15 mL.

On June 30, the FDA labelled this recall as a Class II recall. This means that using the product could lead to temporary health issues, but serious injuries are unlikely. The affected products have expiration dates from July 2026 to October 2026.

People who have these eye drops should check with their healthcare provider or pharmacist. They can find out if their medication is part of the recall and discuss alternative treatments. Patients should not stop their medication without talking to a healthcare provider first.

Lupin started the recall on June 4 and informed customers by letter. The FDA continues to monitor the situation.

How much do you know?

How many bottles of eye medication are being recalled?

1 million

2.5 million

2,530,182

5 million

What is the name of the medication being recalled?

Prednisone

Prednisolone acetate

Ibuprofen

Acetaminophen

What is the purpose of prednisolone acetate ophthalmic suspension?

Pain relief

Treating inflammation after eye surgery

Preventing infections

Reducing redness in eyes

In which country were the recalled bottles made?

United States

India

China

Mexico

What type of recall was issued by the FDA for this medication?

Class I

Class II

Class III

Voluntary

Until what month can the affected products be expired?

June 2026

October 2026

December 2026

January 2027

More than 2.5 million bottles of a prescription eye medication are being recalled.

True False

The FDA classified the recall as a Class I recall.

True False

Lupin Pharmaceuticals Inc. is located in the United States.

True False

Patients should discontinue their medication without consulting a healthcare provider.

True False

The recall began on June 4.

True False

The affected products were sold in sizes of 10 mL and 20 mL.

True False

The FDA raised concerns after finding foreign material in some bottles of .

This suspension treats inflammation after eye surgery and helps with certain eye .

The bottles were sold in different sizes: 5 mL, 10 mL, and .

People who have these eye drops should check with their healthcare provider or .

The affected products have expiration dates from July 2026 to .

The FDA continues to the situation.

This question is required