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ResourcesDynarex Corporation Recalls Product Due to Possible Health Risk
Summary
Company Announcement Date:
September 19, 2024
FDA Publish Date:
September 19, 2024
Product Type:
Cosmetics
Reason for Announcement:
Potential Metal or Chemical Contaminant
Company Name:
Dynarex Corporation
Brand Name:
dynacare
Product Description:
Baby Powder
Company Announcement
Montvale, NJ, September 19, 2024 — Dynarex Corporation is recalling 62 cases of item number 4875, Dynacare Baby Powder, Batch Number B 051, because it has the potential to be contaminated with asbestos. Asbestos is a naturally occurring mineral that is often found near talc, an ingredient in many cosmetic products. Asbestos, however, is a known carcinogen and its health risks are well-documented. During talc mining, if talc mining sites are not selected carefully or steps taken to purify the talc ore sufficiently, the talc may be contaminated with asbestos.
The product was sent to distributors on or after March 11, 2024, by direct delivery in the following states: AL, AR, CO, IL, KY, NC, NJ, PA, TN, FL, WA, WI and sold online on Amazon (Amazon.com).
The 4875 Baby Powder is packaged in 14 oz. plastic bottles, 24 bottles to a case, identified as batch/lot number B051, Expiration Date 2026/12/28 (located on the bottom of the bottle).
There have been no illnesses or adverse events reported to date.
The recall was the result of a routine sampling program by the FDA which revealed that the finished products contained asbestos. The company has ceased the distribution of the product as an investigation is proceeding to determine what caused the contamination of the talc.
Consumers who have purchased Dynacare Baby Powder, Batch Number B 051, should discontinue use immediately and return it for a full refund. Please contact Dynarex Corporation at 888-396-2739 or 845-365-8200 during business hours of 8:30 AM to 5:00 PM Eastern Standard Time, or via email at recall@dynarex.com if you have any questions or need information on how to return the product or receive a full refund.
Health care professionals and consumers are encouraged to report any adverse events to FDA’s MedWatch Adverse Event Reporting program by:
· Complete and submit the report online at MedWatch Online Voluntary Reporting Form
· Downloading and completing the form, then submitting it via fax at 1-800-FDA-0178
Company Contact Information
Product Photos
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* We believe that none of the product being recalled were processed or offered through the national office
* We strongly encourage you to notify your agencies within one business day from receipt of this notice.
* ALL cased and uncased inventories, both at the member level and agency level, need to be checked. This product may have entered member and agency warehouses through salvage, local donations, TEFAP, local purchases, retail pickups, food drives, or other avenues.
* For additional local details, please contact the Health Department(s) for the area(s) your food bank serves.
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About Feeding America Recall Notices
The Feeding America national office issues notifications of all national Class I and II recalls–those involving a health hazard situation in which there is reasonable probability that eating the food will cause health problems or death–and other recalls that may affect the safety of food supplied to network members.
The national office strongly encourages all member product solicitors, operations managers, and others involved in food and grocery distribution to regularly consult resources provided by the United States Food and Drug Administration (FDA) at https://www.fda.gov/opacom/7alerts.html, and the United States Department of Agriculture (USDA) at https://www.fsis.usda.gov/Fsis_Recalls/index.asp. Additionally, members can often receive information on national, state, and local recalls by contacting their local health departments.
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