• U.S. FDA
    Comprehensive Ophthalmology

    Hospira, Inc. is voluntarily recalling 1 lot of vancomycin hydrochloride injection, USP (NDC: 0409-6510-01, Lot 591053A, Expiry Date 1NOV2017) due to a confirmed customer report for the presence of particulate matter in a single vial.

    The product is packaged in a carton containing 1x100 mL vial. The lot was distributed from August 2016 through September 2016 in the United States. Anyone with an existing inventory of the recalled lot should stop use and distribution and quarantine the product immediately.

    Report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

    • Complete and submit the report Online: accessdata.fda.gov/scripts/medwatch
    • Download form 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