CLASS IIIFood recall · Reported 19 Jul 2017 · FDA Enforcement Report
Item 12738 - Apple PIE Burrito, Scrambled Eggs AND Potatoes>24EA/CS recalled
Correctional Industries Food Factory is recalling Item 12738 - Apple PIE Burrito, Scrambled Eggs AND Potatoes>24EA/CS, distributed in Arizona, Montana, Nevada, Oregon, Washington. The recall was initiated on 18 May 2017 and the FDA has classified it as Class III.
Check your package
Lot, batch or date codesno codes, no expiration dates. Mfg dates: April 1, 2017 to May 15, 2017.
Quantity recalled12,927 lbs.
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product is recalled because it was made with water contaminated with chemicals perfluorooctanoic acid (PFOA) and perluorooctanesulfonic acid (PFOS). The observed PFOS and PFOA levels exceed EPA's 2016 combined Lifetime Health Advisory levels for drinking water (70 parts per trillion [ppt]).
Product as listed by the FDA
Item 12738 - APPLE PIE BURRITO, SCRAMBLED EGGS AND POTATOES>24EA/CS, Frozen, Net. Wt. 22.88 lbs. per case
Product is recalled because it was made with water contaminated with chemicals perfluorooctanoic acid (PFOA) and perluorooctanesulfonic acid (PFOS). The observed PFOS and PFOA levels exceed EPA's 2016 combined Lifetime Health Advisory levels for drinking water (70 parts per trillion [ppt]).
Which lots are affected?
no codes, no expiration dates. Mfg dates: April 1, 2017 to May 15, 2017.
Where was it sold?
distribution in AZ, MT, NV, OR, and WA.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.