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FDA recall record

Ferrous Sulfate Tablets 325 mg, 100 count bottles, Nutritional Supplement. Label reads in part "OPTIMUM *** FERROUS SULFATE 325 * mg 5 Grain *** Gluten Free Dietary Supplemen...

Recall F-1304-2013Class IIITerminatedMarch 18, 2013

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 9, 2014. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Ferrous Sulfate Tablets 325 mg, 100 count bottles, Nutritional Supplement. A. *** *325 mg calculated as Ferrous Sulfate Heptahydrate. ***" UPC 0 43292 56306 0 There are 72 bottles per shipping case and most product is shipped by case.

Reason

The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.

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.

  • Ferrous Sulfate Tablets 325 mg, 100 count bottles, Nutritional Supplement. A. *** *325 mg calculated as Ferrous Sulfate Heptahydrate. ***" UPC 0 43292 56306 0 There are 72 bottles per shipping case and most product is shipped by case.

Code information listed by FDA

Product code -L6430-100-01(L is designate label, 6430 is the firm's internal product code, 100 is for 100 count and 01 stands for Optimum label, and 0 is the firm's version number. All of these products have the same label code, however; they have different lot numbers. Lot Numbers: 343617, 343718, 343739, 343753, 343814, 343888, and 343959.

Expiration dates 11/15, 12/15, 12/15, 12/15, 12/15, 1/16 and 1/16 respectively (expiration dates are month and year) The lot number and expiration date is stamped on the bottom of the bottles.

Distribution and firm information

Recalling firm listed by FDA: Magno Humphries Inc

Firm location listed by FDA: Tigard, OR, United States

Distribution reported by FDA: Distributed to only one consignee with several locations nationwide.

Product quantity listed by FDA: 40369 bottles

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.