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Lower risk Drug recall · FDA · Published April 13, 2023

DuPont Nutrition Avicel PH-200 NF Bulk Container Recall: Conductivity Issue

DuPont Nutrition USA recalls bulk Avicel PH-200 NF containers due to failed impurities tests. Check batch numbers for affected units. No immediate action needed for consumers.

🇺🇸 FDA recall #D-0546-2023DrugDuPont Nutrition ›
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Recalling firmDuPont Nutrition USA, Inc1301 Ogletown Rd · Newark, DE 19711-5419
✎ GovInfoNow plain-language explainer

DuPont Nutrition is recalling bulk containers of Avicel PH-200 NF microcrystalline cellulose because tests showed conductivity issues. This is a quality control problem that doesn't affect end users directly. Read more at govinfonow.com/recall/33731-dupont-nutrition-avicel-ph-200-nf-bulk-container-recall-conductivity.

Source Summary by GovInfoNow · govinfonow.com/recall/33731-dupont-nutrition-avicel-ph-200-nf-bulk-container-recall-conductivity · Updated August 17, 2026 · FDA enforcement record: FDA #D-0546-2023

Cite this page

“DuPont Nutrition Avicel PH-200 NF Bulk Container Recall: Conductivity Issue.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/33731-dupont-nutrition-avicel-ph-200-nf-bulk-container-recall-conductivity. Based on FDA recall #D-0546-2023 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0546-2023%22&limit=1).

DuPont Nutrition USA, Inc. recalled Avicel PH-200 NF microcrystalline cellulose on April 13, 2023, due to failed impurity specifications, according to the FDA. The Food and Drug Administration announced the Class III recall.

How to tell if you have it

  • Brand: DuPont Nutrition
  • Product: Avicel PH-200 NF, Microcrystalline Cellulose NF
  • Net Content/Gross Weight: 20.0 KG / 21.1 KG bulk container
  • Batch Numbers: 2173766945, 2173768895, PN20834306, 217373201, PN20834301

The hazard

The recall addresses out-of-specification results obtained for conductivity. The product is classified as Class III.

Context

GovInfoNow's records show DuPont Nutrition USA, Inc. has 3 other recalls on record since 2021-08-05. Other recent recalls of similar products include Shoolin Pharma Chem Tadalafil Recall (2026-08-03), Leading Pharma Recalls Furosemide 80mg Due to Impurity (2026-03-20), and Wells Pharma Fentanyl Citrate Injectable Solution Recall (2026-04-01).

How to tell if you have this one

Check for batch numbers 2173766945, 2173768895, PN20834306, 217373201, or PN20834301 on the container. The product is a bulk container with net weight 20.0 kg or gross weight 21.1 kg.

  • Brand
    DuPont Nutrition
  • Category
    Drug
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class III
  • Status
    Terminated
  • Distribution
    Nationwide in the USA, Malta, Canada, China, Peru, Mexico, Australia, Saudi Arabia, Spain, Dominican Republic, Puerto Rico, Singapore, Bangkok, Ireland, India, and Columbia.
Recall numberProduct, codes & lotsQuantity
D-0544-2023Avicel PH-101 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 50.0 KG / 54.5 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark.; Batch Numbers: 2173809472, 2173811313, P120834282, P120834305, P120834313, P120834324, P120834423, P120834437, P120834443, P120834478, 2173739298, 2173740020, 2173771315, P120834254, P120834476464,050 kg in bulk drums, boxes & sacks
D-0545-2023Avicel PH-102 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark.; Batch Numbers: P220834360, P220834366, P220834383, P220834440, P220834460, 2173755143, 2173771316, 2173773188, P220834401, P220834403, P220834482, P220834505, P220834543, P220834545320,350 kg in bulk drums, boxes & sacks
D-0546-2023Avicel PH-200 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark.; Batch Numbers: 2173766945, 2173768895, PN20834306, 217373201, PN2083430193,660 kg in bulk drums, boxes & sacks
D-0547-2023Avicel DG, MCC/Dibasic Calcium Phosphate, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark.; Batch Numbers: 2213749659, 2213766837, 2213776558, 221377655923,060 kg in bulk drums, boxes & sacks
Based on the official FDA remedy

What to do — step by step

  1. Check Batch Numbers

    Look for batch numbers 2173766945, 2173768895, PN20834306, 217373201, or PN20834301 on the container.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Nationwide in the USA, Malta, Canada, China, Peru, Mexico, Australia, Saudi Arabia, Spain, Dominican Republic, Puerto Rico, Singapore, Bangkok, Ireland, India, and Columbia.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Apr 13, 202312. FDA classified it Class III: Apr 25, 202323. Published in FDA’s Enforcement Report: May 3, 202334. FDA terminated the recall: Mar 4, 2024420232024
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #D-0546-2023 (April 13, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0546-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA