FDA Food recall F-1244-2013
All-In-One Probiotics, K12-BB12-LB3
- FDA Food
- Class II
- terminated
- Published 2013-03-27
On 2013-03-27 the FDA classified a Class II recall of All-In-One Probiotics, K12-BB12-LB3 by Wynlife Healthcare, citing wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1244-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-05-31 |
| Published | 2013-03-27 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | Wynlife Healthcare |
| Distribution | US |
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
Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.
Identifiers
| code_info | PN 141; Lot #'s: 100521 and 110099 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1244-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.