DuPont Nutrition USA, Inc: Drug Recall
Recall #D-0352-2023 · 02/01/2023
Class III: Low Risk
Recall Details
- Recall Number
- D-0352-2023
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- DuPont Nutrition USA, Inc
- Status
- Terminated
- Date Initiated
- 02/01/2023
- Location
- Newark, DE, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 106,560 kg. polyethylene lined fiber drums, boxes & sacks
Reason for Recall
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Product Description
BD-102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp., 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. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark
Distribution Pattern
Product was distributed nationwide in the United States and Puerto Rico, and to Australia, China, Canada, Columbia, Mexico, Brazil, Malaysia, Chile, Dominic Republic, Singapore, Thailand, Ireland, Germany, South Korea, Argentina, Pakistan, Oman, India
Other Recalls by DuPont Nutrition USA, Inc
- Class III: Low Risk 04/13/2023
- Class III: Low Risk 04/13/2023
- Class III: Low Risk 04/13/2023
- Class III: Low Risk 04/13/2023
- Class III: Low Risk 02/01/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.