All-In-One Probiotics — Class II food recall F-1244-2013
Terminated recall by Wynlife Healthcare, Inc., reported 2013-03-27, distributed nationwide. Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contamina
| Recall number | F-1244-2013 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wynlife Healthcare, Inc., San Diego, CA, United States |
| Recall initiated | 2011-05-31 |
| Classified | 2013-03-21 |
| Reported by FDA | 2013-03-27 |
| Terminated | 2013-03-21 |
| Distributed | Nationwide (US) |
| Quantity | 456 boxes |
| Lot numbers | 100521, 110099 |
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. Manufactured for Wynlife Healthcare, Inc., San Diego, CA 92130.
Reason for recall
Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1244-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.