FDA Drug Recalls

Recalls / Class III

Class IIID-0352-2023

Product

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

Affected lot / code info
Batch # 2173784100, B220834549 These excipients are noted not to have an expiration date.

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Recalling firm

Firm
DuPont Nutrition USA, Inc
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1301 Ogletown Rd, N/A, Newark, Delaware 19711-5419

Distribution

Quantity
106,560 kg. polyethylene lined fiber drums, boxes & sacks
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

Timeline

Recall initiated
2023-02-01
FDA classified
2023-02-24
Posted by FDA
2023-03-08
Terminated
2023-12-20
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0352-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.