Routine sampling uncovers asbestos, prompting recall across 35 states
In a significant safety alert, the U.S. Food and Drug Administration (FDA) has expanded the recall of Dynacare Baby Powder to 35 states after detecting asbestos contamination. The baby powder, which was being sold through Amazon and in retail outlets across various states, was flagged during routine testing conducted by the FDA.
Initial recall and expansion
Originally, the recall began in 12 states last month but has now been extended following further sampling results. The recalled baby powder was distributed in states including California, Texas, Florida, New York, and Illinois, among others. Consumers who have purchased the product are advised to discontinue use immediately and return it for a full refund. The recall affects both 14-ounce and 4-ounce sizes.
Health risks associated with asbestos
Asbestos, a known carcinogen, can pose severe health risks when inhaled or ingested. It is a naturally occurring mineral that is sometimes found near talc deposits, raising the risk of contamination if mining and purification are not meticulously managed. “If talc mining sites are not carefully chosen or if proper steps are not taken to adequately purify the talc ore, it may contain asbestos,” the FDA explained.
Company response and investigation
Dynacare has ceased the distribution of its baby powder and is cooperating with an ongoing investigation to determine the source of the contamination. Although no illnesses have been publicly reported, the company urges all customers to return the product for a refund as a precautionary measure.
How to request a refund
Customers seeking information on refunds and product returns can reach Dynarex Corporation by calling 888-396-2739 or 845-365-8200 during regular business hours (8:30 a.m. to 5 p.m. ET), or via email at recall@dynarex.com.
The FDA continues to monitor the situation and stresses the importance of adhering to recall notices to ensure consumer safety.
