El Encanto recalls GC Medium 5-5# Z pouches (Product Item 1055-3) due to possible Listeria monocytogenes contamination. Affected units include Lot 2813, 5 lbs each in cardboard boxes.
Products were recalled due to possible Listeria monocytogenes contamination.
El Encanto is recalling GC Medium 5- 5# Z food pouches (Product Item 1055-3) because they may contain Listeria monocytogenes. This bacteria can cause serious illness, so affected consumers should stop using these products.
Listeria monocytogenes is a bacteria that can cause severe food poisoning. It is particularly dangerous for pregnant women, newborns, and people with weakened immune systems, as it can lead to miscarriage, stillbirth, or life-threatening infections.
Consumers who purchased GC Medium 5-5# Z pouches (Product Item 1055-3) from El Encanto. Those with compromised immune systems are at higher risk for serious illness.
Check for GC Medium 5-5# Z pouches with Product Item Number 1055-3. The product comes in sealed poly film pouches inside cardboard boxes with a shipper label. Lot 2813 is the affected batch.
Discard all GC Medium 5-5# Z pouches with Product Item Number 1055-3 and Lot 2813 immediately.
No, the product may contain Listeria monocytogenes, which can cause serious illness. Do not consume.
Product Item Number 1055-3, Lot 2813.
Look for GC Medium 5-5# Z pouches with Product Item Number 1055-3 and Lot 2813 in sealed poly film pouches inside cardboard boxes.
We’ve drafted a message you can send El Encanto to request your refund or repair — edit it as you like.
Subject: Recall F-1510-2014 — El Encanto El Encanto Hello, I own a El Encanto that is covered by recall F-1510-2014 from El Encanto. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.