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Firvanq (vancomycin hydrochloride for oral solution), Vancomycin 50 mg/mL Kit, Each Kit Includes: 1 bottle containing 7.7 g Vancomycin Hydrochloride USP, powder for oral solution and 1 bottle containing 145 mL Grape Flavored Diluent for reconstitution per carton, Rx only, Manufactured for: Azurity pharmaceuticals, Wilmington, MA 01887, NDC 65628-206-05.

Drug Recall

Official source record

Recall number
D-0003-2022
Event ID
88547
Classification
Class I
Status
Terminated
Recalling company
Azurity Pharmaceuticals, Inc.
Reason for recall
Product Mix-up: Incorrect diluent component included in the kit.
Report date
October 13, 2021
Recall initiation date
August 24, 2021
Termination date
May 12, 2022
Distribution pattern
USA nationwide

Drug product identifiers

Manufacturer
Azurity Pharmaceuticals, Inc
Brand name
FIRVANQ
Generic name
VANCOMYCIN HYDROCHLORIDE
Product NDCs
65628-204; 65628-205; 65628-206; 65628-208
Package NDCs
65628-204-05; 65628-205-10; 65628-206-05; 65628-208-10

Where this information comes from

View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this medication?

Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.

Where can I find more official information?

The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.