Grove Fresh Pasteurized Apple Juice from concentrate, 4-ounce cartons, 100 % Pure.
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1567-2017.
The firm received several customer complaints regarding foreign material in the product. The firm tested seven of the returned product units and found that they were positive for undeclared milk. The product has been recalled due to undeclared milk.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1567-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Dairy Maid Dairy, Llc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1567-2017.
Dairy Maid Dairy, LLC
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Dairy Maid Dairy, Llc Recall FAQ
Dairy Maid Dairy, Llc is the subject of a beverages safety report: Grove Fresh Pasteurized Apple Juice from concentrate, 4-ounce cartons, 100 % Pure.. The notice was published on February 16, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.