VitaminAlly Joint Nourish liquid recalled over manufacturing practice deviations
VitaminAlly Joint Nourish oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen contamination and possible C. botulinum concerns.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall where the manufacturing deviations are described as potentially leading to bacterial pathogen contamination, a named risk of harm with no illnesses reported.
Plain-English summary
Joint Nourish, an oral liquid supplied in a 480 ml plastic bottle with a 2 tablespoon (30 ml) dose, from VitaminAlly LLC of Chandler, Arizona, is being recalled. The action covers 90 bottles.
The stated reason is deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. botulinum concerns. The FDA classified the action as Class II.
The affected lot is JN0925, expiry 09/2027, distributed between 1 October 2025 and 8 April 2026. Distribution was nationwide and to Puerto Rico.
Consumers who have the affected lot should stop using it and dispose of it or return it to the place of purchase. Anyone who has used it and feels unwell should contact a healthcare provider.
The recalled product
- Product
- Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
- Manufacturer
- Wellnov Supplements LLC
- Category
- Food — Dietary supplement
- Affected units
- 90
Distribution
Part of a larger recall action
This product is one of 14 recalled by Wellnov Supplements LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 14 products in this recall →Related recalls
Same manufacturer · Wellnov Supplements LLC
See all →- HighVitaminAlly iron-free women's multivitamin drops recalled over manufacturing deviations
FDA (Food) · 2026-05-27
- HighVitaminAlly liposomal D3 and B12 spray recalled over manufacturing deviations
FDA (Food) · 2026-05-27
- HighVitaminAlly womens 50+ multivitamin drops recalled over manufacturing deviations
FDA (Food) · 2026-05-27
- HighVitaminAlly kids liquid multivitamin drops recalled over manufacturing deviations
FDA (Food) · 2026-05-27
- HighVitaminAlly liposomal B12 spray recalled over manufacturing practice deviations
FDA (Food) · 2026-05-27
Same hazard · cgmp deviation
See all →- SevereZicam Cold Remedy Nasal Swabs Recalled for Microbiological Testing Failures
FDA (Drugs) · 2026-09-02
- ModerateGolden State Medical Supply Recalls Carbamazepine Tablets Due to CGMP Deviations
FDA (Drugs) · 2026-08-26
- SevereShoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
FDA (Drugs) · 2026-08-19
- ModerateShoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
FDA (Drugs) · 2026-08-19
- HighShoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
FDA (Drugs) · 2026-08-19