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Class III: unlikely to cause harmTerminated

DuPont Nutrition Avicel Recall

Avicel, Mirocrystalline cellulose, packaged in bulk as PH101 NF, PH102 NF, PH200 NF, Ma…

DuPont Nutrition USA, Inc · Newark, DE

Risk level
Class III
Reported by FDA
Aug 25, 2021
Recall ID
D-0728-2021
Check your lot numberHow we source this data

Summary

DuPont Nutrition recalled Avicel starting Aug 5, 2021. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0728-2021 on Aug 25, 2021. Reason: Out of specification results for conductivity. Status: Terminated.

Why it was recalled

Out of specification results for conductivity.

Product description

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

Lot numbers, UPCs & expiration codes

Lot Numbers: P120834253, PN20834314, PN20834326, P220834329, P120834471, 2173728724, 2173731307, 2173739294, 2173742956, 2173743721, 2173747040 217374970, 2173749846, 2173751395, 2173751995, 2173753080, 2173749460, 2173755135, 2173755142, 2173758869, 22173758869 2173759101, 2173759087, 2173760958, 21737606959, 2173762248, 217376233, 2173763871 2173763872, 2173755139, 2173763875, 2173764734, 2173763870, 2173764735, 2173769670, 2173775381, 2173776518, 217377536, 2173779284, 2173800414, 2173801736, 2173801737, 2173802516, 2173805796, 2173805797, 2173806449, 2173806450, 2173809474, 2173809473 2173810873, 2173811314, 2173811315, 2173806441, 217381169, 2173811666 These excipients are noted not to have an expiration date.

Where it was sold

Product was distributed nationwide, including Puerto Rico and to foreign accounts abroad.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0728-2021
Classification
Class III
Status
Terminated
Recall initiated
Aug 5, 2021
FDA report date
Aug 25, 2021
Quantity
2,384,720 kg
Recall type
Voluntary: Firm initiated
Recalling firm
DuPont Nutrition USA, Inc

Original FDA data

Every field from FDA enforcement report D-0728-2021, exactly as published.

Show all FDA fields
City
Newark
State
DE
Status
Terminated
Country
United States
Event ID
88428
Address
1301 Ogletown Rd
Code information
Lot Numbers: P120834253, PN20834314, PN20834326, P220834329, P120834471, 2173728724, 2173731307, 2173739294, 2173742956, 2173743721, 2173747040 217374970, 2173749846, 2173751395, 2173751995, 2173753080, 2173749460, 2173755135, 2173755142, 2173758869, 22173758869 2173759101, 2173759087, 2173760958, 21737606959, 2173762248, 217376233, 2173763871 2173763872, 2173755139, 2173763875, 2173764734, 2173763870, 2173764735, 2173769670, 2173775381, 2173776518, 217377536, 2173779284, 2173800414, 2173801736, 2173801737, 2173802516, 2173805796, 2173805797, 2173806449, 2173806450, 2173809474, 2173809473 2173810873, 2173811314, 2173811315, 2173806441, 217381169, 2173811666 These excipients are noted not to have an expiration date.
Postal code
19711-5419
Report date
Aug 25, 2021
Product type
Drugs
Recall number
D-0728-2021
Classification
Class III
Recalling firm
DuPont Nutrition USA, Inc
Product quantity
2,384,720 kg
Termination date
Mar 7, 2023
Reason for recall
Out of specification results for conductivity.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Product was distributed nationwide, including Puerto Rico and to foreign accounts abroad.
Recall initiation date
Aug 5, 2021
Initial firm notification
Letter
Center classification date
Aug 16, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0728-2021, published Aug 25, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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