Wynlife Recalls Vegi-Fiber Plus and Probiotics Due to DEHP Contamination
Wynlife Healthcare is recalling Vegi-Fiber Plus and All-In-One Probiotics because they contain DEHP-contaminated clouding agents.
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 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which indicates a situation where use of the product could cause temporary or medically reversible health consequences. There are no reported illnesses or injuries in the source text.
Plain-English summary
Wynlife Healthcare, Inc. is recalling its Vegi-Fiber Plus and All-In-One Probiotics products. The recall is being conducted because the products contain clouding agents that are contaminated with DEHP.
The affected Vegi-Fiber Plus products are dietary supplements sold in 60-packet boxes. The specific items involved are identified by Product Number 135 and Lot Numbers 090336 and 100340. A total of 210 boxes were distributed nationwide.
Consumers who have these products should stop using them and contact Wynlife Healthcare for further instructions.
The recalled product
- Product
- Vegi-Fiber Plus; O Trans Fat; only 15.4 Calories; Dietary Supplement; 60 Packets; Scientific formula for Natural Vitality; 15 Vegetable and Fruit Extracts; Newest Japanese Carbohydrate Blocker: Fibersol -2; Each Packet Contains 3.5g of Water-Soluble Dietary Fiber. Manufactured…
- Manufacturer
- Wynlife Healthcare, Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 210
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 (2)
- PN 135
- Lot #'s: 090336 and 100340
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Wynlife Healthcare, Inc. 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 2 products in this recall →Related recalls
Same manufacturer · Wynlife Healthcare, Inc.
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