Recall archive / FDA company announcement

Crecelac: Powdered Goat Milk Infant Formula — FDA announcement Jun 4, 2024

Published notice; closure not supplied

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 Jun 4, 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: Powdered Goat Milk Infant Formula
Reason: Cronobacter spp. contamination
Classification: Not supplied
Recalling firm: Dairy Manufacturers Inc.
Quantity: Not supplied
Agency-reported status: Company recall announcement
Source record identifier: fbb6e203331d9ef4

Open the official record

Lot and product identifiers

Label field	Details supplied by the agency
Lot, code or applicability	Dairy Manufacturers Inc., of Prosper, TX – 6/3/24, is notifying consumers about a safety issue associated with a product that is an extension of an ongoing voluntary recall (https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dairy-manufacturers-inc-issues-voluntary-recall-products-due-non-compliance-requirements-under-21). D-M initiated a voluntary recall on 05/24/24. Crecelac Infant 0-12 with an expiration date of 08/2025 was manufactured at D.M. Mexicana Sa De Cv in Monterey, Mexico and is part of this ongoing recall. D-M is now alerting consumers that a sample of this product has tested positive for Cronobacter spp.; Only the lot listed below had samples containing Cronobacter spp.; The recalled product can be identified by the batch code on the bottom of the can.; PRODUCT \| UPC \| LOT CODE \| EXP. DATE; Crecelac Infant 0-12 \| 8 50042 40847 6 \| 24 039 1 CHE 352-1 \| 08/2025

Label field

Details supplied by the agency

Lot, code or applicability

Dairy Manufacturers Inc., of Prosper, TX – 6/3/24, is notifying consumers about a safety issue associated with a product that is an extension of an ongoing voluntary recall (https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dairy-manufacturers-inc-issues-voluntary-recall-products-due-non-compliance-requirements-under-21). D-M initiated a voluntary recall on 05/24/24. Crecelac Infant 0-12 with an expiration date of 08/2025 was manufactured at D.M. Mexicana Sa De Cv in Monterey, Mexico and is part of this ongoing recall. D-M is now alerting consumers that a sample of this product has tested positive for Cronobacter spp.; Only the lot listed below had samples containing Cronobacter spp.; The recalled product can be identified by the batch code on the bottom of the can.; PRODUCT | UPC | LOT CODE | EXP. DATE; Crecelac Infant 0-12 | 8 50042 40847 6 | 24 039 1 CHE 352-1 | 08/2025

Match all identifying details in the current notice. A brand name alone is not enough.

Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

FDA company announcement, table 1
PRODUCT	UPC	LOT CODE	EXP. DATE
Crecelac Infant 0-12	8 50042 40847 6	24 039 1 CHE 352-1	08/2025

Announcement retrieved Oct 1, 2026. Official announcement.

Distribution

Crecelac 12.4 oz containers were distributed primarily in March, April, and May of 2024. The product was distributed through retail stores in the state of Texas only. The recalled product is labeled as infant formula and packaged in a 12.4 oz. cardboard and aluminum can.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Texas

Dates in the source

Fda listing date: Jun 4, 2024
Company announcement date: Jun 3, 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.