Up&Up Psyllium Fiber Supplement — Class II drug recall D-025-2013

Terminated recall by Raritan Pharmaceuticals, Inc., reported 2012-10-31, distributed nationwide. Microbial Contamination of Non-Sterile Products: Product is being recalled due to possible microbial contamina

Recall number	`D-025-2013`
Product type	Drug
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Raritan Pharmaceuticals, Inc., East Brunswick, NJ, United States
Recall initiated	2012-09-04
Classified	2012-10-25
Reported by FDA	2012-10-31
Terminated	2014-10-07
Distributed	Nationwide (US)
Quantity	48,120 bottles
Reason classes	microbial contamination, sterility
UPC / GTIN / UDI-DI	`00368163119268`
NDC	`11673-0059-87`
Lot numbers	`06/15`, `07/15`, `08/15`, `15952`, `16459`, `16460`, `16463`, `16475`
Model numbers	`119160TGT`

Product

Up&Up Psyllium Fiber Supplement, 100% natural psyllium husk, Fiber Therapy for Regularity/Fiber Supplement, 160 capsules per bottle, Distributed by: Target Corp., Minneapolis, MN 55403, Made in USA, NDC 11673-059-87, UPC 3-68163-11926-8.

Reason for recall

Microbial Contamination of Non-Sterile Products: Product is being recalled due to possible microbial contamination by C. difficile discovered in the raw material.

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/D-025-2013. 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.