Ciranda recalls Organic Carob Powder Light (Product Code 20030) due to Salmonella contamination found in one lot. Consumers should check their purchases for this specific product and follow safety steps.
Ciranda is recalling one lot of Organic Carob Powder Light after learning that a customer received a positive test for Salmonella.
Ciranda is recalling one lot of Organic Carob Powder Light (Product Code 20030) because a customer tested positive for Salmonella. This poses a food safety risk as Salmonella can cause serious illness if consumed.
Salmonella is a bacteria that can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. In rare cases, it can cause serious illness, especially in vulnerable individuals such as young children, elderly people, or those with weakened immune systems.
Anyone who purchased Ciranda Organic Carob Powder Light (Product Code 20030) from a retailer. People with compromised immune systems are at higher risk from Salmonella infections.
Check for the product code 20030 on the packaging. The product was manufactured in Italy and sold with a lot number of 395-13. This specific lot was recalled due to a positive Salmonella test.
Look for the product code 20030 on the packaging to confirm if you have the recalled item.
No, the recalled lot has been tested positive for Salmonella, which can cause food poisoning. Do not consume this product.
The recall record does not specify any remedy or replacement options.
The recall record does not provide specific instructions for disposal or return. Check with the manufacturer or retailer for guidance.
We’ve drafted a message you can send Ciranda to request your refund or repair — edit it as you like.
Subject: Recall F-2334-2014 — Ciranda Ciranda Hello, I own a Ciranda that is covered by recall F-2334-2014 from Ciranda. 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.
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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.
