• Voluntary recall of IMOVAX® Rabies Vaccine lot numbers X0667-2, X0667-3, W1419-2, and W1419-3. Information about this recall is available from the Aventis Pasteur Medical Information Services Department, telephone 800-835-3587, or at http://www.vaccineshoppe.com.
    
• Recall of Meningococcal Polysaccharide Vaccine, Groups A, C, Y, W-135 Combined, single-dose vials (including single-dose in five dose packaging), Menomune - Aventis Pasteur - 10/18/2002. Additional information regarding the Menomune recall:

	Printable format
	Addendum with list of recalled lots (.pdf format) Statement from Vaccine Manufacturer (.pdf format)
	Text-only format for screen-reader devices
	Addendum with list of recalled lots (.rtf format) Statement from Vaccine Manufacturer (.rtf format)

• Recall of Hepatitis A Vaccine, Inactivated (VAQTA) (Packaged in single-dose prefilled syringes for International Distribution) (Merck & Co, Inc.) - 2/7/2002

• Recall of Hepatitis A Vaccine, Inactivated (VAQTA) - (Merck & Co., Inc) - 12/10/2001

• Voluntary Recall of Rabies Vaccine, RabAvert) - (Chiron Behring GmbH & Co) - 3/16/2001

• Voluntary Recall of Hepatitis B Vaccine (Recombinant), Engerix-B - (Glaxo SmithKline Beecham) - 2/22/2001

• Voluntary Recall of Diphtheria & Tetanus Toxoids Adsorbed - (Bioport Corp) - 9/1/2000

• Voluntary Recall of Anthrax Vaccine Adsorbed - (Bioport Corp) - 8/30/2000 - (Clarification)

• Firm Initiated Recall of Haemophilus b Conjugate (HibTITER) - (Wyeth-Ayerst Pharmaceutical) - 8/30/2000

• Recall of Rabies Vaccine, IMOVAX Rabies I.D. - (Aventis Pasteur S.A.) - 7/28/2000

• Withdrawal of Rotavirus Vaccine, Live, Oral, Tetravalent (RotaShield) - (Wyeth Laboratories, Inc.) - 10/15/1999

• Firm Initiated Recall of Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed - (Connaught Laboratories, Inc.) - 1/27/1999

Top of page