FDA recall record

Oregon Freeze Dry Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham recall — FDA F-2087-2014

Oregon Freeze Dry, Inc. is voluntarily recalling Mountain House Scrambled Eggs with Ham and Red & Green Peppers due to undeclared wheat, soy and coconut.…

Class IIclassification
F-2087-2014official record ID
Jul 16, 2014report date

Recall record at a glance

Official recordF-2087-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmOregon Freeze Dry, Inc.
Report dateJul 16, 2014
Recall initiation dateJun 11, 2014
Quantity248 cans (Mixture of correctly and incorrectly labeled cans)
LocationAlbany, OR, United States

Official product description

Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in #10 metal can. Product is labeled in part "***INGREDIENTS: Precooked Scrambled Eggs* (whole eggs, egg yolk, nonfat dry milk, modified corn starch, corn oil, salt, yeast extract, sunflower oil, smoke flavoring, xanthan gum). Ham* (ham, salt, dextrose, sodium tripolyphosphate, sodium erythorbate, smoke flavor, sodium nitrite), Red and Green Peppers*. *Freeze Dried CONTAINS: Milk, Egg.***OREGON FREEZE DRY, INC***ALBANY, OR***"

Why the product was recalled

Oregon Freeze Dry, Inc. is voluntarily recalling Mountain House Scrambled Eggs with Ham and Red & Green Peppers due to undeclared wheat, soy and coconut. Canned product has the potential to be mislabeled and actually contain Mountain House Granola with Milk and Blueberries.

Distribution information

Product was distributed in the United States to: AL, AR ,AZ, CA, CO, CT ,DE, FL, ID, IL, IN, KY, MI, MN, MO, MS, NC, NE, NV, NY, OH, OR, PA, SC, RI, TN, TX, UT, VA, and WV. No foreign distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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