FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Leader Liquid Vitamin D Supplement for Breastfed Infants, 1…
- Published
- September 20, 2017
- Distribution
- Nationwide
The Harvard Drug Group Recall: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
United States
TerminatedClass II
- Company
- The Harvard Drug Group
- Product
- Rugby Cerovite Liquid, 8 oz. 236ML
- Recall date
- August 2, 2017
- Terminated
- April 28, 2020
- Source
- FDA
Reason for recall
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Rugby Cerovite Liquid, 8 oz. 236ML | Not published in this source record | 65,611 units | Rugby Cerovite Liquid, 236ML, UPC Number: 00536-2790-59, All Unexpired Lots |
Distribution
- Domestic: Nationwide to USA Foreign: None VA/DOD: VA CMOP CHARLESTON 3725 RIVERS AVE N. CHARLESTON SC 29405-7038
- Ph. 303-339-4305
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-3516-2017
- Event ID
- 78007
- Status
- Terminated
- Classification
- Class II
- Company
- The Harvard Drug Group
- Product description
- Rugby Cerovite Liquid, 8 oz. 236ML
- Quantity
- 65,611 units
- Reason
- The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
- Recall initiation date
- August 2, 2017
- Report date
- September 20, 2017
- Classification date
- Not published in this source record
- Termination date
- April 28, 2020
- Distribution pattern
- Domestic: Nationwide to USA Foreign: None VA/DOD: VA CMOP CHARLESTON 3725 RIVERS AVE N. CHARLESTON SC 29405-7038, Ph. 303-339-4305
- UPC, lot, and code information
- Rugby Cerovite Liquid, 236ML, UPC Number: 00536-2790-59, All Unexpired Lots
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78007 with 10 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Leader Liquid Multivitamin Supplement for Infants and Toddle…
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Major Tri-Vita Drops, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Major Poly-Vita Drops with Iron, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Major Poly-Vita Drops, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Major Ferrous Drops, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Major D-Vita Drops, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Major CertaVite Liquid, 8 oz. (236 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Rugby Tri-vitamin Liquid, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
The Harvard Drug Group
- Product
- Rugby Polyvitamin Liquid with Iron, 1 2/3 oz (50 mL)
- Published
- September 20, 2017
- Distribution
- Nationwide
Responsible company: The Harvard Drug Group
Other recalls from The Harvard Drug Group
FDA Recall Terminated Historical recordClass II
Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count Tablets Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-7179-61
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Gabapentin Tablets, USP 600 mg, packaged in Cartons of 100 tablets (10 tablets per blister pack x 10), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. East Windsor, NJ 08520 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA, NDC 0904-6823-61
- Published
- May 17, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Carbidopa and Levodopa Tablets, USP 25 mg/100 mg, 10x10 Unit Dose carton, Rx Only, Manufactured in Czech Republic by: Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Manufactured for: Teva Pharmaceuticals USA, Inc. Parsippany, NJ 07054, Packaged and Distributed by: Major Pharmaceuticals Indianapolis, IN 46268 USA. NDC 0904-7257-61, UPC 3 09047 25761 4
- Published
- March 8, 2023
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Virginia | 1 |
| South Carolina | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
