FDA recall record

Organics Corporation of America DBA Ambix NaturesPlus Advanced Therapeutics Glucosamine recall — FDA D-0559-2022

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.

Class IIclassification
D-0559-2022official record ID
Feb 23, 2022report date

Recall record at a glance

Official recordD-0559-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOrganics Corporation of America DBA Ambix Laboratories
Report dateFeb 23, 2022
Recall initiation dateDec 6, 2021
Quantity4,214 tubes
LocationTotowa, NJ, United States

Official product description

NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz tubes, Manufactured for NaturesPlus 548 Broadhollow Road, Melville, NY 11747, USA

Why the product was recalled

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.

Distribution information

The product went to one consignee. Natural Organics, Inc., 548 Broadhollow Rd., Melville, NY 11747.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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