Johnson & Johnson recalls 574,000 bottles of anti-fever medicines for children in the United States**

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On the 17th, the US Johnson & Johnson announced that after receiving complaints from parents regarding bottle design issues, the company decided to recall 573,000 bottles of grape-flavored antipyretic Tylenol oral liquids sold in the US market.

Johnson & Johnson said that the recalled drugs were just listed in November last year and were produced by the company's pharmaceutical factory in Italy. They are mainly used for infants under two years of age. In order to ensure accurate medication, the bottle body adopts a new design. However, the company has received complaints from 17 parents saying that the protective cap dropped into the bottle when the straw was inserted into the vial.

Johnson & Johnson said that this recall will focus on retail pharmacies and wholesalers. For consumers, if the protective cap on the top of the bottle is still in use, it can continue to use the drug. In addition, Tylenol for children over the age of two is not included in this recall.

Johnsons spokesman Bonnie Jacobs said that the company has so far received no reports of serious adverse reactions to recalled drugs, and the risk of such problems is also "very small."

In the past two years or more, there have been many drug recalls by Johnson & Johnson and some of its subordinate pharmaceutical factories still have unhealthy conditions. The US Food and Drug Administration has warned this.

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