O Organics Vegetable Tray, 18 oz. (1 lb. 2 oz.) 510g plastic tray. Best If Used By: AUG 11 UPC (incorrect, which is on the tray): 02113...
⚠ 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-2338-2016.
Incorrect ingredient label was attached to 18 oz. O Organics vegetable Trays with Creamy Ranch Dressing Dip and therefore do not correctly identify the allergens egg, milk and soy.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2338-2016.
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 Mann Packing Company, Inc. 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-2338-2016.
Mann Packing Company, Inc.
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.
Mann Packing Company, Inc. Recall FAQ
Mann Packing Company, Inc. is the subject of a produce safety report: O Organics Vegetable Tray, 18 oz. (1 lb. 2 oz.) 510g plastic tray. Best If Used By: AUG 11 UPC (incorrect, which is on the tray): 02113.... The notice was published on August 4, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 844 units are potentially affected.