Data Foundry

Drug recalls 2021

Avicel — Class III drug recall D-0728-2021

Terminated recall by DuPont Nutrition USA, Inc, reported 2021-08-25, distributed nationwide. Out of specification results for conductivity.

Recall numberD-0728-2021
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmDuPont Nutrition USA, Inc, Newark, DE, United States
Recall initiated2021-08-05
Classified2021-08-16
Reported by FDA2021-08-25
Terminated2023-03-07
DistributedNationwide (US)
Quantity2,384,720 kilograms
Reason classesspecification failure
Lot numbers2173728724, 2173731307, 2173739294, 2173742956, 2173743721, 2173747040, 2173749460, 217374970, 2173749846, 2173751395, 2173751995, 2173753080, 2173755135, 2173755139, 2173755142, 2173758869, 2173759087, 2173759101, 21737606959, 2173760958, 2173762248, 217376233, 2173763870, 2173763871, 2173763872, 2173763875, 2173764734, 2173764735, 2173769670, 217377536, 2173775381, 2173776518, 2173779284, 2173800414, 2173801736, 2173801737, 2173802516, 2173805796, 2173805797, 2173806441 and 15 more

Product

Avicel, Mirocrystalline cellulose, packaged in bulk as PH101 NF, PH102 NF, PH200 NF, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711

Reason for recall

Out of specification results for conductivity.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0728-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.