CORRECTING and REPLACING Teva Pharmaceuticals Initiates Voluntary Nationwide Recall of Seven Lots of Amikacin Sulfate Injection USP 500mg/2 mL (250 mg/mL) and 1 gram/4 mL (250 mg/mL) Vials Due to Potential of Glass Particulate Matter

Please replace the release dated July 29, 2016 with the following corrected version due to changes in the paragraph immediately following the table listing the recalled lots.

The corrected release reads:

TEVA PHARMACEUTICALS INITIATES VOLUNTARY NATIONWIDE RECALL OF SEVEN LOTS OF AMIKACIN SULFATE INJECTION USP 500MG/2 ML (250 MG/ML) AND 1 GRAM/4 ML (250 MG/ML) VIALS DUE TO POTENTIAL OF GLASS PARTICULATE MATTER

Teva Pharmaceuticals today announced a voluntary recall of seven lots of Amikacin Sulfate Injection USP, 500 mg/2mL (250 mg/mL) and 1 gram/4mL (250 mg/mL) vials due to the potential for the presence of glass particulate matter. The recalled lots are:

The administration of a glass particulate, if present in an intravenous drug, may result in local irritation or swelling in response to the foreign material. More serious potential outcomes would include blockage and clotting in blood vessels, which may be life-threatening if a critical organ is affected. To date, Teva has not received any reports of adverse events or complaints related to this recall.

Amikacin Sulfate Injection USP is used in the short-term treatment of serious infections due to susceptible strains of Gram-negative bacteria, and has also been shown to be effective in staphylococcal infections and may be considered as initial therapy under certain conditions in the treatment of known or suspected staphylococcal disease. Amikacin Sulfate Injection belongs to a class of medications called aminoglycoside antibiotics and is supplied as 2 mL and 4 mL vials packaged in shelf pack of 10 500 mg/2 mL (250 mg/mL) and 1gram/4 mL (250 mg/mL) vials. Amikacin Sulfate Injection 250 mg/mL, 2 mL & 4 mL vials were distributed nationwide through wholesalers, retailers, and pharmacies.

Teva has issued an Urgent Drug Recall Letter to their direct customers. Teva is arranging for impacted product to be returned to Inmar. Anyone with an existing inventory of the recalled lot(s) should stop use and distribution, and quarantine the product immediately. Customers should notify all retail and medical facility accounts. Customers who have further distributed the recalled product should notify any accounts or additional locations which may have received the recalled product and instruct them if they have redistributed the product to notify their accounts, locations or facilities.

For medical related questions please contact Teva Medical Information at 888-838-2872, option 3, then, option 4. For a customer service related question, please contact Teva Customer Service at 800-545-8800, Monday – Friday; 8:00 AM – 5:00 PM EST. Consumers should immediately contact their physician or healthcare provider if they have experienced any problems that may be related to taking this drug product. For product quality complaint-related questions please contact Teva Quality Assurance Services at 888-838-2872, option 3, then, option 3.

Adverse reactions experienced with the use of this product may be reported to Teva Pharmaceuticals at 1-888-838-2872, option 3, then option 4. Adverse Events or product quality issues experienced with this product can also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Complete and submit the report Online: www.fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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