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Drug recall records

Sodium Chloride recall records

Review openFDA enforcement records that match Sodium Chloride, then compare the product description, manufacturer, NDC, and lot or code information with your package.

74 matching sodium chloride enforcement records found.

Coverage is September 23, 2024 through September 23, 2026, last checked September 23, 2026. A drug-name match alone does not mean every product or package is affected.

Class I

Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured by: Gland Pharma Limited, Hyderabad, - 500 043 INDIA, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, NDC 43598-636-52

Dr. Reddy's Laboratories, Inc.

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.

D-0365-2025

April 23, 2025

How to check a Sodium Chloride record

  1. Confirm the exact generic or brand name and dosage form.
  2. Compare the manufacturer, strength, and package size.
  3. Match the NDC and lot, batch, or other code information.
  4. Open the record and use the linked FDA source to verify the details.
Do not stop or change a prescribed medication based only on this page. Contact a pharmacist or prescriber if you are concerned about a specific product.

This page is generated from public openFDA Drug Enforcement records. It is not an FDA service and does not determine whether a medicine in your possession is recalled.