The Harvard Drug Group — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 22, 2026, The Harvard Drug Group has 18 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 2 Aug 2017. The Harvard Drug Group is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for The Harvard Drug Group
How serious are The Harvard Drug Group recalls?
FDA recall classifications by severity
Full FDA recall history for The Harvard Drug Group
All 18 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 2 Aug 2017Official FDA Notice | Major Ferrous Drops, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Major CertaVite Liquid, 8 oz. (236 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Tri-vitamin Liquid, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Major Poly-Vita Drops, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Leader Liquid Multivitamin Supplement for Infants and Toddlers , 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Polyvitamin Liquid with Iron, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Calcionate Syrup, One Pint (473 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Major Poly-Vita Drops with Iron, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Leader Liquid Vitamin D Supplement for Breastfed Infants, 1 T oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Major D-Vita Drops, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Ferrous Sulfate Liquid One Pint, (473 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Liquid Vitamin C Supplement, 4 oz., 118 mL | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Cerovite Liquid, 8 oz. 236ML | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Major Tri-Vita Drops, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby D 3 Vitamin Liquid, 400 IUI/1 mL, 1 and 2/3 oz., 50 mL | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 2 Aug 2017Official FDA Notice | Rugby Polyvitamin Liquid, 1 2/3 oz (50 mL) | The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recal | Class IITerminated |
| 31 Dec 2014Official FDA Notice | Thera Tablets with Beta Carotene Dietary Supplement | The firm received a complaint that the blister packets were missing labeling information on 12/16/2014, the firm investigated the labeling complaint a | Class IIITerminated |
Where have The Harvard Drug Group recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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