Food Recall Check
Class III · Low risk Terminated Initiated Dec 31, 2014 (12 years ago)

Thera Tablets with Beta Carotene Dietary Supplement recall

Recalled by The Harvard Drug Group, LLC · Livonia, MI, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

The firm received a complaint that the blister packets were missing labeling information on 12/16/2014, the firm investigated the labeling complaint and found that six 2 x 5 blister cards inside a carton was missing some or all of the product information on the back of the blister card.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Thera Tablets with Beta Carotene Dietary Supplement

Quantity: 5,700 unit doses 10 x 10 cartons

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Number: M-00953 Expiration Date: 06-2015, UPC Code: 3 09040 53961 8

Where it was sold

Alabama Arizona California Colorado Connecticut Florida Georgia Illinois Kentucky Massachusetts Michigan Missouri Mississippi North Carolina Nebraska New Jersey New York Ohio Oregon Pennsylvania Tennessee Texas Utah Virginia Washington Wisconsin West Virginia

FDA's distribution note: Domestic: AL, AZ, CA, CO, CT, FL, GA, IL, KY, MA, MI, MO, MS, NC, NE NJ, NY, OH, OR, PA, TN, TX, UT, VA, WA, WI, WV. Foreign: None Foreign:

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
The Harvard Drug Group, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 31, 2014
In FDA report of
Feb 4, 2015
Terminated
Mar 9, 2016
FDA recall number
F-0925-2015 · event 70171
Official record
FDA enforcement report search

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