---
title: "NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint... — FDA record D-0559-2022 | Is It on Recall"
description: "MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae."
url: https://isitonrecall.com/recall/fda-drug-d-0559-2022-naturesplus-advanced-therapeutics-glucosamine-chondroitin-msm-ultra-rx-joint-cream-4-oz-tubes-manufa/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz tubes, Manufactured for Nat... — FDA record D-0559-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 6, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz tubes, Manufactured for NaturesPlus 548 Broadhollow Road, Melville, NY 11747, USA
- **Reason**: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.
- **Classification**: Class II
- **Recalling firm**: Organics Corporation of America DBA Ambix Laboratories
- **Quantity**: 4,214 tubes
- **Agency-reported status**: Ongoing
- **Source record identifier**: D-0559-2022

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0559-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Product code 4929, Lot # 23622 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Feb 23, 2022
- **Recall initiation date**: Dec 6, 2021
- **Center classification date**: Feb 14, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0559-2022%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Organics Corporation of America DBA Ambix Laboratories records](https://isitonrecall.com/brand/organics-corporation-of-america-dba-ambix-laboratories/)