VitaminAlly liposomal collagen booster recalled over manufacturing practice deviations
VitaminAlly Liposomal Collagen Booster is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen 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
Liposomal Collagen Booster, 90 ml in an aluminium bottle, from VitaminAlly LLC of Chandler, Arizona, is being recalled. The action covers 49 bottles.
The stated reason is deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. botulinum concerns. The FDA classified the action as Class II.
The affected lot is CB0625, expiry 06/2027, distributed between 1 June 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
- Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
- Manufacturer
- Wellnov Supplements LLC
- Category
- Food — Dietary supplement
- Hazard
- cgmp-deviation
- bacterial-pathogen
- clostridium-botulinum
- class-ii
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Distribution Dates: 06/01/2025-04/08/2026 Lot Number CB0625 Expiry Date 06/2027
Distribution
Distributed nationwide across the United States.
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