Onions Red Rings 3/16 (item 78267) sold by 5 lb bag for foodservice use, perishable, refrigerated, shelf life 5 days, packed in 5 lbs. ce...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). 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-1271-2020.
Processed onions products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International Inc.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1271-2020.
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 Emerald Fruit & Produce 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-1271-2020.
Emerald Fruit & Produce 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.
Emerald Fruit & Produce Inc Recall FAQ
Emerald Fruit & Produce Inc is the subject of a produce safety report: Onions Red Rings 3/16 (item 78267) sold by 5 lb bag for foodservice use, perishable, refrigerated, shelf life 5 days, packed in 5 lbs. ce.... The notice was published on July 31, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 55 units are potentially affected.