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Dr. Reddy's Laboratories, Inc.: Levetiracetam 0.75% in Sodium Chloride

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: LABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL, while the aluminum overwrap packaging correctly identifies the product as Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL.. Recalled by Dr. Reddy's Laboratories, Inc.. Distribution: Nationwide in the USA. Classification (Class I — serious health hazard). Affected lots/NDC/dates: Lot: A1540076, Exp 08/31/2026. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who purchased the recalled drug or medication. Return it to the pharmacy where you bought it for a full refund. You generally do not need the original receipt — the pharmacist can look up your purchase history.
Source Official Source ↗
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