China has repeatedly vowed tighter oversight and crackdowns on
companies and officials after food and drug safety scandals sparked
public outrage, such as one last month over expired polio vaccines
and another last year over a rabies vaccine.
Human immunoglobulin, made with human blood plasma, is used to treat
a variety of conditions, but it was not clear how many people might
have been injected from the suspect batch, which media said
consisted of 12,226 units, due to expire in 2021.
Tests on the suspect batch proved negative for HIV, officials said
late on Wednesday, following a comment by China's National Health
Commission that there was a "very low" risk of HIV infection from
it.
The Shanghai Medical Products Administration said in a statement the
batch, which health authorities identified as number 20180610Z, was
made by China Meheco Xinxing Pharma Co, a unit of state-controlled
China Meheco Group Co Ltd.
Reuters could not immediately reach the manufacturer on Thursday to
seek comment. Most offices in China are shut for the week-long Lunar
New Year holiday.
Domestic media outlet the China Economic Observer said the
investigation began after an HIV test on a baby in southeastern
Jiangxi province initially yielded a "weak" positive result that was
traced to the batch under investigation.
Subsequently, the baby tested negative for HIV, it added.
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"Shanghai authorities have run virus tests for HIV, hepatitis B and
hepatitis C on the reported batch and they all show negative," the
National Medical Products Administration said in a statement on
Wednesday.
of the batch and seal remaining supplies for further investigation.
Shanghai's Medical Products Administration said it had ordered the
manufacturer to halt production.
Last month, China's National Medical Products Administration asked
manufacturers to add warnings against potential risks from
intravenously injected human immunoglobulin and frozen human
immunoglobulin products, saying the raw materials derived from human
blood.
In 2016, the Shanghai medical products regulator warned the same
company over changes to the manufacturing process for some human
fibrinogen products without assessing potential risks, the
regulator's website showed.
(Reporting by Muyu Xu and Tony Munroe; Editing by Michael Perry and
Clarence Fernandez)
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