FDA recall record
Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 28, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL
Code information listed by FDA
Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL, UPC Number: 00536-0710-80, All Unexpired Lots
Distribution and firm information
Recalling firm listed by FDA: The Harvard Drug Group
Firm location listed by FDA: Livonia, MI, United States
Distribution reported by FDA: Domestic: Nationwide to USA Foreign: None VA/DOD: VA CMOP CHARLESTON 3725 RIVERS AVE N. CHARLESTON SC 29405-7038, Ph. 303-339-4305
Product quantity listed by FDA: 27,011 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.