US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 4, 2012 (14 years ago)

Up&Up Psyllium Fiber Supplement

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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.

Recalling firm
Raritan Pharmaceuticals, Inc.
NDC code
11673-059-87
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-025-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Psyllium recalls

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Class III · Low risk Terminated

Psyllium Fiber

Reason Labeling: Label Error on Declared Strength; Listed active ingredient strength is inaccurate.

Konsyl Pharmaceuticals Inc D-1315-2014
Class II · Moderate risk Terminated

DRxChoice Fiber Capsules

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

Raritan Pharmaceuticals, Inc. D-032-2013
Class II · Moderate risk Terminated

Premier Value Fiber Capsules

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

Raritan Pharmaceuticals, Inc. D-030-2013
Class II · Moderate risk Terminated

Simply Right Healthcare Fiber Capsules

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

Raritan Pharmaceuticals, Inc. D-029-2013
Class II · Moderate risk Terminated

Berkley & Jensen Fiber Capsules

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

Raritan Pharmaceuticals, Inc. D-028-2013