Major Ferrous Drops, 1 2/3 oz (50 mL)
Recalling firm: The Harvard Drug Group
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 28, 2020.
Check your package
Compare the exact product and package details with the label you have.
309046273509FDA code information
Major Ferrous Drops,1 2/3 oz (50 mL), UPC Number:3 09046 27350 9, All Unexpired Lots
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Major Ferrous Drops, 1 2/3 oz (50 mL)
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 309046273509 | Major Ferrous Drops,1 2/3 oz (50 mL), UPC Number:3 09046 27350 9, All Unexpired Lots |
Original FDA recall 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 details
- Recall number
- F-3526-2017
- Event ID
- 78007
- FDA status
- Terminated
- Initiated
- Aug 2, 2017
- Reported
- Sep 20, 2017
- Classified
- Sep 12, 2017
- Terminated
- Apr 28, 2020
- Quantity
- 63,005 units
- Location
- Livonia, MI, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
Domestic: Nationwide to USA Foreign: None VA/DOD: VA CMOP CHARLESTON 3725 RIVERS AVE N. CHARLESTON SC 29405-7038, Ph. 303-339-4305
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.