VitaminAlly prenatal multivitamin drops recalled over manufacturing practice deviations
VitaminAlly Liposomal Prenatal+Postnatal Liquid Multivitamin Drops, iron free, are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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 Prenatal+Postnatal Liquid Multivitamin Drops, Iron Free, 90 ml in an aluminium bottle, from VitaminAlly LLC of Chandler, Arizona, is being recalled. The action covers 25 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 PN0824, expiry 08/2026, distributed between 1 September 2024 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 Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225
- Manufacturer
- Wellnov Supplements LLC
- Category
- Food — Dietary supplement
- Affected units
- 25
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: 09/01/2024-04/08/2026 Lot Number PN0824 Expiry Date 08/2026
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
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