Class II · Moderate risk Ongoing
Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%
Reason cGMP deviations and lack of assurance of sterility.
Bd-102 Nf
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
What was recalled
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
- Recalling firm
- DuPont Nutrition USA, Inc
- Origin
- DE, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0352-2023
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Cellulose recalls
See all
Class II · Moderate risk Ongoing
Carboxymethylcellulose Sodium Ophthalmic Gel 1%
Reason cGMP deviations and lack of assurance of sterility.
Class III · Low risk Ongoing
Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%…
Reason LABELING: LABEL MIX-UP
Class I · High risk Ongoing
Up&Up brand dry eye relief
Reason Non-Sterility
Class I · High risk Ongoing
Lubricant Gel Drops
Reason Non-Sterility
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