FDA Recalls Over 4 Million Tubes of Indian-Made Toothpaste
- Reports
- 5
- Developments
- 1
- Repetition
- 80%
New informationRepeats or wire copies
What happened
The Food and Drug Administration (FDA) recalled more than 4 million tubes of toothpaste nationwide. The recall affects 17 different toothpaste products, including those marketed for children. These products were manufactured by Pritam International Private Limited in India and distributed in the U.S. by Ashtel Studios Inc. The recall was initiated on September 10 due to deviations from Current Good Manufacturing Practice (CGMP).
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Why it matters
The FDA assigned the recall a Class II risk level for the possibility of temporary or reversible health effects. This action impacts the sales and distribution of the affected consumer health products and disrupts the supply chain for these imports into the United States.
An alert regarding a product recall originated in the manufacturer's country, involving India.
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Who's involved
- FDARegulatory agency that issued the recall.
- United States of AmericaThe market where the recalled products were distributed.
Who could feel it
Possible knock-on effectsThese are possibilities Brind reasoned out, not predictions, and not advice. Most are not stated in any report.
- FDASpeculative
Pritam International Private Limited could face reduced revenue due to the recall of its products.
Possible ripples
Who this could reach next, traced step by step from the reporting. Possibilities worth considering, not forecasts.Keep exploring
The entities involved
Related events
- The Food and Drug Administration (FDA) oversees product safety and recalls.
- The FDA has posted a nationwide recall notice.
- The FDA has listed recalled products, involving the company Colgate.
- Neogen Corporation, a company operating in the US market, is facing action from the FDA concerning a product recall.
- The FDA classified the recall of Great Value items, which were distributed in New Mexico, Louisiana, Alabama, and Pennsylvania.