Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class II · Moderate risk Ongoing Initiated Dec 6, 2021 (5 years ago)

NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

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

Drug: Glucosamine

Recalling firm
Organics Corporation of America DBA Ambix Laboratories
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0559-2022 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Glucosamine recalls

See all
Class II · Moderate risk

GLUCOSAMINE/CHONDROITIN Capsule

Labeling:Label Mixup; GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg may be potentially mislabeled as FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: AD60240_30, EXP: 5/22/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-616-2014
Class II · Moderate risk

Glucosamine/Chondroitin Ds

Labeling: Label Mixup; GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD60211_11, EXP: 5/22/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-484-2014

Other microbial contamination recalls from 2021

All microbial contamination recalls
Class II · Moderate risk

Betaxolol Ophthalmic Solution

Microbial Contamination of Sterile Products: Confirmed sterility failure identified during stability testing at the 12-month time point.

Terminated Microbial contamination Akorn, Inc. NDC 17478-705-11 D-0004-2022
Class II · Moderate risk

Valproic Acid Oral Solution

CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.

Terminated Microbial contamination American Health Packaging D-0854-2021