Joint Nourish Recall Issued by Wellnov Supplements LLC
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Wellnov Supplements LLC is recalling 90 bottles of Joint Nourish liquid supplement distributed nationwide and in Puerto Rico due to cGMP deviations that could lead to bacterial contamination.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 11, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, supplements.
What Happened
Wellnov Supplements LLC has initiated a voluntary recall of Joint Nourish liquid due to deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.
Which Products Are Affected
The recall involves Joint Nourish liquid (2 tablespoons/30mL dosage, for oral use) packaged in 480 ml plastic bottles. A total of 90 bottles are affected, with lot number JN0925 and expiry date 09/2027. Distribution dates were 10/01/2025-04/08/2026. Products were distributed nationwide and in the United States Territory of Puerto Rico.
What You Should Do
Consumers should not use the recalled product. Contact information for returns or refunds is not specified in the recall notice.
Why This Matters
This Class II recall addresses potential contamination risks from manufacturing deviations in a dietary supplement distributed across the United States and Puerto Rico.
Source
FDA recall number H-0795-2026 (event ID 98832).
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,023 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to June 11, 2026.
Frequently Asked Questions
Common questions about this FDA recall.