Recall archive / FDA company announcement
dynacare: Baby Powder — FDA announcement Sep 19, 2024
Reported terminated
A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.
Source date Sep 19, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Baby Powder
- Reason
- Potential Metal or Chemical Contaminant
- Classification
- Not supplied
- Recalling firm
- Dynarex Corporation
- Quantity
- Not supplied
- Agency-reported status
- Terminated in FDA listing
- Source record identifier
- e3770f9fbd9f9edd
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 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 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).; 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 [email protected] if you have any questions or need information on how to return the product or receive a full refund. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
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).
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Fda listing date
- Sep 19, 2024
- Company announcement date
- Sep 19, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.