VBI Vaccines Issues Voluntary Nationwide Recall of all PreHevbrio Vaccine Due to Discontinuation of Company Operations

CAMBRIDGE, Mass. — VBI Vaccines Inc. (VBI) is initiating a voluntary nationwide recall of all remaining PreHevbrio^® [Hepatitis B Vaccine (Recombinant); NDC 75052-001-10] (“PreHevbrio”) due to the bankruptcy of the company and termination of operations.

Further distribution or use of any remaining PreHevbrio vaccine by healthcare providers or others must cease immediately.

VBI Vaccines Inc. and its affiliates commenced a proceeding under Canada’s Companies’ Creditors Arrangement Act, R.S.C. 1985, c. C-36, as amended (the “CCAA Proceeding”) on July 29, 2024, in the Superior Court of Justice (Commercial List) in Ontario, Canada. VBI Vaccines (Delaware) Inc. and certain other affiliates filed petitions and a motion under chapter 15 of the Bankruptcy Code for recognition of the Canadian Proceeding as a foreign main proceeding on July 30, 2024, in the United States Bankruptcy Court for the District of Delaware (together with the CCAA Proceeding, the “Restructuring Proceedings”). In connection with the Restructuring Proceedings, on October 25, 2024, the company issued an initial communication to healthcare providers and the FDA regarding its intent to voluntarily withdraw PreHevbrio from the U.S. market. The company is rapidly winding down all U.S. operations and has permanently ceased distribution of PreHevbrio, a vaccine indicated for the prevention of infection caused by hepatitis B virus in adults.

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PreHevbrio vaccine was distributed nationwide to distributors and healthcare providers.

COMMUNICATION AND REQUEST FOR DESTRUCTION OF INVENTORY:

VBI Vaccines is notifying its distributors, clients, and healthcare providers by direct mail and is requesting that they further notify or re-notify any potentially affected customers, consumers, and/or patients of this recall. VBI Vaccines is requesting immediate destruction of all existing vials of PreHevbrio in accordance with applicable law, and notification of product disposition to [email protected].

The U.S. Food and Drug Administration is aware that VBI has permanently discontinued distribution of PreHevbrio.

ADVERSE EVENT REPORTING:

Adverse reactions or possible side effects experienced in connection with the use of PreHevbrio may be reported to Vaccine Adverse Event Reporting System (“VAERS”) either online, by fax, or by regular mail.

• Complete and submit the report Online: https://vaers.hhs.gov/
• Regular Mail or Fax: Download PDF form ( https://vaers.hhs.gov/) and fax to 1-877-721-0366, or mail the completed form to:

VAERS
P.O. Box 1100
Rockville, MD, 20849-1100

If you require assistance with reporting, you can contact VAERS by email at [email protected] or by phone at 1-800-822-7967.

INTERCHANGEABILITY AND SERIES COMPLETION:

For healthcare providers needing to complete a Hepatitis B vaccination series when the original vaccine administered is no longer available, please refer to the Centers for Disease Control (CDC) Hepatitis B vaccination guidelines at https://www.cdc.gov/hepatitis-b/hcp/vaccine-administration/.

HOW TO IDENTIFY PREHEVBRIO:

Please visit www.prehevbrio.com for vial and carton labels as well as information about unexpired lots of PreHevbrio.

ADDITIONAL QUESTIONS:

Healthcare providers and distributors with questions regarding this recall can contact VBI Vaccines at [email protected]. Consumers who received PreHevbrio should reach out to their physicians or other qualified healthcare providers with any questions or concerns related to the use of PreHevbrio.

View source version on businesswire.com: https://www.businesswire.com/news/home/20241115135978/en/

Contacts

[email protected]

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