DuPont Nutrition USA recalls Avicel PH-200 NF microcrystalline cellulose due to failed impurities tests. This ingredient is used in pharmaceuticals and may not meet safety standards.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
DuPont Nutrition is recalling Avicel PH-200 NF microcrystalline cellulose because it failed impurities and degradation tests. This ingredient is used in pharmaceuticals and could pose safety risks if not properly controlled.
The product failed impurities and degradation tests, meaning it may contain harmful substances or break down in ways that could affect drug safety. This is a quality control issue that could lead to unsafe pharmaceutical products.
Pharmaceutical manufacturers using this ingredient in drug production are likely affected. Those handling the product without proper quality checks may be at risk.
Check for the product name 'Avicel PH-200 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp' with net content 20.0 KG or 21.1 KG bulk. The batch numbers PN20834322 and PN20834335 are associated with this recall.
Verify the product name, net content, and batch numbers to confirm if it's part of this recall.
The recall indicates the product failed impurities and degradation tests, so it may not meet safety standards. Do not use without confirming it's not recalled.
The recall does not specify a remedy, so check the product details to see if it's affected. Contact DuPont Nutrition USA for further guidance.
Look for the product name 'Avicel PH-200 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp' with net content 20.0 KG or 21.1 KG bulk and batch numbers PN20834322 or PN20834335.
We’ve drafted a message you can send DuPont Nutrition to request your refund or repair — edit it as you like.
Subject: Recall D-0351-2023 — DuPont Nutrition DuPont Nutrition Hello, I own a DuPont Nutrition that is covered by recall D-0351-2023 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.
