F-1244-2013 Class II Terminated
FDA food recall F-1244-2013 was initiated by Wynlife Healthcare, Inc. on May 31, 2011 and is designated Class II. Reason for recall: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents. The recall status is terminated (terminated March 21, 2013). Affected quantity: 456 boxes.
Recall Details
- Product Type
- Food
- Report Date
- March 27, 2013
- Initiation Date
- May 31, 2011
- Termination Date
- March 21, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 456 boxes
Product Description
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.
Distribution Pattern
Nationwide distribution.
Code Information
PN 141; Lot #'s: 100521 and 110099