Florida Included in Nationwide Baby Powder Recall Over Asbestos Contamination

Recalled baby powderPhoto byFDA press release

Dynarex Corporation has issued an urgent recall for 62 cases of Dynacare Baby Powder due to potential contamination with asbestos, a known carcinogen. The affected product, identified as batch number B051, was distributed to multiple states, including Florida, and sold online through Amazon.

The recall involves 14-ounce plastic bottles of Dynacare Baby Powder, packaged in cases of 24, with an expiration date of December 28, 2026. The recall follows an FDA routine sampling program that detected asbestos contamination in the talc-based product. Talc is often found near asbestos deposits, and without careful mining practices, contamination can occur.

The potentially hazardous baby powder was shipped to distributors across 12 states, including Florida, and was available for purchase on Amazon. Distribution began on March 11, 2024. Although no illnesses or adverse events have been reported at this time, consumers are urged to stop using the product immediately and return it for a full refund.

Asbestos is a naturally occurring mineral linked to severe health issues, particularly cancers such as mesothelioma when inhaled. According to health experts, even small amounts of exposure can be dangerous over time. In response, Dynarex has ceased further distribution of the product and is currently investigating the source of contamination.

What Consumers Should Do
Consumers who purchased Dynacare Baby Powder, batch number B051, are advised to:

• Discontinue use immediately.
• Contact Dynarex Corporation for instructions on returning the product and receiving a full refund.

For assistance, consumers can reach Dynarex Corporation at:

• Phone: 888-396-2739 or 845-365-8200 (8:30 AM to 5:00 PM EST, Monday–Friday)
• Email: recall@dynarex.com

Reporting Health Issues
Although no adverse reactions have been reported, anyone who experiences health issues after using the product is encouraged to contact their healthcare provider. Additionally, consumers and medical professionals can report adverse effects to the FDA’s MedWatch program:

• Online: MedWatch Online Voluntary Reporting Form
• Fax: 1-800-FDA-0178

For more details and the latest updates on the recall, visit the FDA’s website or contact Dynarex Corporation directly.

Product photoPhoto byFDA press release