CLASS III Food recall · Reported 4 Feb 2015 · FDA Enforcement Report
Thera Tablets with Beta Carotene Dietary Supplement recalled
The Harvard Drug Group is recalling Thera Tablets with Beta Carotene Dietary Supplement, distributed in 27 states. The recall was initiated on 31 Dec 2014 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0925-2015
- FDA event ID
- 70171
- Recalling firm
- The Harvard Drug Group, Livonia, MI
- Brand
- Thera
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 31 Dec 2014
- FDA classified
- 23 Jan 2015
- Reported
- 4 Feb 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
- Product category
- Dietary Supplements
Timeline
| 31 Dec 2014 | Recall initiated by company | |
| 23 Jan 2015 | Classified by FDA | +23 days |
| 4 Feb 2015 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Product as listed by the FDA
Thera Tablets with Beta Carotene Dietary Supplement
Where it was distributed
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:
AlabamaArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIllinoisKentuckyMassachusettsMichiganMissouriMississippiNorth CarolinaNebraskaNew JerseyNew YorkOhioOregonPennsylvania
Questions about this recall
Why was it 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.
Which lots are affected?
Lot Number: M-00953 Expiration Date: 06-2015, UPC Code: 3 09040 53961 8
Where was it sold?
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:
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |