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High RiskFDAfda-F-0465-2020OTHER

Plant Based WayFare Butterscotch Pudding Organic Dairy Free, Item #1223. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard ove...

Category
Units Affected
4,699
Recall Date
December 13, 2019
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0465-2020.

Product is recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0465-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Wayfare Health Foods Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0465-2020.

Wayfare Health Foods LLC

FDA

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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📣 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.

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Wayfare Health Foods Llc Recall FAQ

Wayfare Health Foods Llc is the subject of a dairy safety report: Plant Based WayFare Butterscotch Pudding Organic Dairy Free, Item #1223. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard ove.... The notice was published on December 13, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 4,699 units are potentially affected.