DuPont Nutrition USA recalls Avicel PH-102 NF microcrystalline cellulose due to failed impurities tests. This product is used in pharmaceuticals and may not meet safety standards.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
DuPont Nutrition USA is recalling Avicel PH-102 NF microcrystalline cellulose because it failed impurities and degradation tests. This product is used in pharmaceutical manufacturing and may not meet safety standards.
The product failed impurities and degradation specifications, resulting in conductivity measurements outside acceptable limits. This could indicate potential safety issues in pharmaceutical products that use this ingredient.
Pharmaceutical manufacturers using this product for drug formulations are likely affected. Those handling the product without proper quality checks may be at risk.
Check for the product name 'Avicel PH-102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp' with net content of 20.0 KG or 21.1 KG bulk. The batch numbers listed include 2173747038 through 220834543.
Identify the product name and batch numbers listed in the recall notice to determine if your product is affected.
The recall indicates the product failed impurities and degradation tests, so it may not meet safety standards. The official notice does not specify if it is safe to use.
The recall does not provide specific action steps for affected products. The official notice does not state what to do if you have the product.
Check for the product name 'Avicel PH-102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp' with net content of 20.0 KG or 21.1 KG bulk and batch numbers listed in the recall notice.
We’ve drafted a message you can send DuPont Nutrition to request your refund or repair — edit it as you like.
Subject: Recall D-0350-2023 — DuPont Nutrition DuPont Nutrition Hello, I own a DuPont Nutrition that is covered by recall D-0350-2023 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.
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.
