The Recall Desk
ModerateFDA (Food)·F-1244-2013·Announced 2013-03-27

Wynlife Recalls Probiotics and Vegi-Fiber Plus Due to DEHP Contamination

Wynlife Healthcare is recalling All-In-One Probiotics and Vegi-Fiber Plus products because they contain DEHP-contaminated clouding agents.

What this means for you

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 typically indicates a situation where use of the product could cause temporary or medically reversible health consequences. No specific injuries or illnesses are reported in the source text.

Plain-English summary

Wynlife Healthcare, Inc. is recalling its All-In-One Probiotics and Vegi-Fiber Plus products. The recall is being conducted because the products contain DEHP-contaminated clouding agents.

The affected products include All-In-One Probiotics (K12-BB12-LB3) in 30-packet boxes. The specific product number is 141, and the affected lot numbers are 100521 and 110099. A total of 456 boxes were distributed nationwide.

Consumers who have these products should stop using them and contact Wynlife Healthcare, Inc. for further instructions or a refund.

The recalled product

Product
All-In-One Probiotics, K12-BB12-LB3; Dietary Supplement; 30 Packets;Serving size 2 Tablets (1 Packet)l L141/1. Adults take 2 to 4 tablets daily; Children: take 1 to 2 tablets daily (or as directed by your healthcare practitioner. Chew slowly or allow to dissolve in mouth. Manufac
Manufacturer
Wynlife Healthcare, Inc.
Category
Food — Dietary Supplement
Hazard
Affected units
456

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 141
  • Lot #'s: 100521 and 110099

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 →

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