Mixed Apples And/or Oranges, sold under brand Fast & Fresh Grab some goodness Product is a combination of Fuji Apples, Granny Smith A...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). 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-1296-2015.
Mixed Apples And/or Oranges, Fast & Fresh Grab some goodness brand, is recalled because it contains Bidart's Granny Smith apples that have been implicated in a Listeria monocytogenes outbreak
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1296-2015.
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 Washington Harvest Wapato 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-1296-2015.
Washington Harvest Wapato
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.
Washington Harvest Wapato Recall FAQ
Washington Harvest Wapato is the subject of a food safety report: Mixed Apples And/or Oranges, sold under brand Fast & Fresh Grab some goodness Product is a combination of Fuji Apples, Granny Smith A.... The notice was published on January 16, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 1,142 units are potentially affected.