Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported February 23, 2022
NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz tubes, Manufactured for NaturesPlus 548 Broadhollow Road, Melville, NY 11747, USA
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.
Organics Corporation of America DBA Ambix Laboratories recalled NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz… - a moderate-severity action.
NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz… was recalled by Organics Corporation of America DBA Ambix Laboratories in February 23, 2022. Reason: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.. Check the official notice for the remedy. Verify recall #D-0559-2022 with the FDA Drug before acting.
The recall
Organics Corporation of America DBA Ambix Laboratories issued this moderate-severity FDA Drug recall-MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae..
- Moderate
- severity level
- Class II
- classification
- February 23, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0559-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0559-2022) was formally reported on February 23, 2022, with the manufacturer initiating the action on December 6, 2021. It is classified under Moderate severity (Class II), with a current status of Ongoing. Organics Corporation of America DBA Ambix Laboratories is listed as the recalling firm, operating out of Totowa, NJ. Federal records list the affected scope as 4,214 tubes.
The documented reason for this recall is: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae. Distribution data in the federal record shows the product reached: The product went to one consignee. Natural Organics, Inc., 548 Broadhollow Rd., Melville, NY 11747.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Cosmetics & Personal Care recalls over time
Where this recall sits in its category - 1,371 cosmetics & personal care recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
4,214 tubes
Related Recalls
6
3 from same agency
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
Reason for recall
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0559-2022 |
| Date reported | February 23, 2022 |
| Date initiated | December 6, 2021 |
| Recalling firm | Organics Corporation of America DBA Ambix Laboratories |
| Firm location | Totowa, NJ |
| Affected scope | 4,214 tubes |
| Distribution | The product went to one consignee. Natural Organics, Inc., 548 Broadhollow Rd., Melville, NY 11747. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0559-2022) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product 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. Recalled by Organics Corporation of America DBA Ambix Laboratories. Units affected: 4,214 tubes.
Why was this product recalled? ▼
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 23, 2022. Severity: Moderate. Recall number: D-0559-2022.
Where was the recalled product distributed? ▼
Distribution: The product went to one consignee. Natural Organics, Inc., 548 Broadhollow Rd., Melville, NY 11747..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0559-2022) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nationwide recalls with similar severity or category timing
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Cosmetics & Personal Care · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
Showing 5 of 1387 other recalls in this category.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported February 23, 2022. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.