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According to the U.S. Food and Drug Administration (FDA), Merck & Co.'s subsidiary Merck Sharp & Dohme Corp. has voluntarily recalled hepatitis B vaccine since June 26, because the drug There may be small amounts of vial crumbs.
The number of hepatitis B vaccine recalled was J001183, which belongs to adult use and has a specification of 10 μg/ml.
This batch of vaccine was introduced into the market between March 12 and May 2, 2013. The self-inspection by Merck discovered that there was a potential for fragmentation of the vaccine vial, which could lead to problems with the safety and sterility of the vaccine.
The supply of hepatitis B vaccine will not be affected by this storm. J001183 is the only group of vaccines that have warts and only appears in the U.S. market.
Consumers should not use J001183 batch vaccine and follow the Merck product recall process. Consumers who already use this lot of vaccine do not need to be re-vaccinated.