The Costco product is sold under brand name Townsend Farms Organic Antioxidant Blend - The product is a mix of IQF organic berries, speci...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (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-0701-2014.
Harris Teeter Organics Antioxidant Berry Blend (10 oz.) and Townsend Farms Organic Antioxidant Blend (3 lbs.) are recalled because it has the potential to be contaminated with Hepatitis A virus, based on the epidemiological and traceback investigation by the FDA and the CDC, of an illness outbreak.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0701-2014.
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 Townsend Farms 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-0701-2014.
Townsend Farms 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.
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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.
Townsend Farms Inc Recall FAQ
Townsend Farms Inc is the subject of a produce safety report: The Costco product is sold under brand name Townsend Farms Organic Antioxidant Blend - The product is a mix of IQF organic berries, speci.... The notice was published on June 3, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 504,060 units are potentially affected.