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High RiskFDAfda-F-0006-2019OTHER

Oregon Heritage Farms Family Blend Apple Cider, 100% Juice, 1 gallon plastic container, UPC: 8 53581 00202 0. The label is read in par...

Category
Units Affected
1,632
Recall Date
September 18, 2018
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0006-2019.

Oregon Heritage Farms Family Blend Apple Cider, 1 gallon size, is recalled due to elevated level of patulin.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0006-2019.

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 Oregon Heritage Developments Inc Dba Oregon Heritage Farms 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-0006-2019.

Oregon Heritage Developments Inc dba Oregon Heritage Farms

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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Oregon Heritage Developments Inc Dba Oregon Heritage Farms Recall FAQ

Oregon Heritage Developments Inc Dba Oregon Heritage Farms is the subject of a beverages safety report: Oregon Heritage Farms Family Blend Apple Cider, 100% Juice, 1 gallon plastic container, UPC: 8 53581 00202 0. The label is read in par.... The notice was published on September 18, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 1,632 units are potentially affected.