DuPont Nutrition USA recalls bulk Avicel DG containers due to conductivity issues. Affected products have specific batch numbers and were manufactured in the USA. Consumers should contact DuPont for details.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
DuPont Nutrition USA is recalling certain bulk Avicel DG containers because they failed impurities and degradation tests. This could pose a risk if the product is used in sensitive applications where impurities affect performance.
The product failed conductivity tests, indicating impurities or degradation. This could lead to inconsistent performance in applications where precise chemical properties are critical, such as in pharmaceutical manufacturing.
Users of these bulk containers in industrial or pharmaceutical settings may be affected. Those handling the product without proper quality checks are at higher risk.
Check for batch numbers: 2213749659, 2213766837, 2213776558, or 2213776559. The product is a bulk container with net weight 20.0 KG and gross weight 21.1 KG, manufactured in the USA by DuPont Nutrition USA, Inc.
Reach out to DuPont Nutrition USA, Inc. for specific instructions on handling the recalled product.
Batch numbers 2213749659, 2213766837, 2213776558, and 2213776559.
Check for the specific batch numbers listed and the product's net weight of 20.0 KG and gross weight of 21.1 KG, manufactured in the USA by DuPont Nutrition USA, Inc.
The recall record does not specify a remedy, so contact DuPont Nutrition USA, Inc. for guidance.
We’ve drafted a message you can send DuPont Nutrition to request your refund or repair — edit it as you like.
Subject: Recall D-0547-2023 — DuPont Nutrition DuPont Nutrition Hello, I own a DuPont Nutrition that is covered by recall D-0547-2023 from DuPont Nutrition. 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.
