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Class III: unlikely to cause harmTerminated

Magno Humphries Ferrous Sulfate Tablets 325 mg Recall

Ferrous Sulfate Tablets 325 mg, 100 count bottles, Nutritional Supplement

Magno Humphries Inc · Tigard, OR

Risk level
Class III
Reported by FDA
Apr 17, 2013
Recall ID
F-1304-2013
Check your lot numberHow we source this data

Summary

Magno Humphries recalled Ferrous Sulfate Tablets 325 mg starting Mar 18, 2013. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1304-2013 on Apr 17, 2013. Reason: The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic. Status: Terminated.

Why it was recalled

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

Product description

Ferrous Sulfate Tablets 325 mg, 100 count bottles, Nutritional Supplement. Label reads in part "OPTIMUM *** FERROUS SULFATE 325 * mg 5 Grain *** Gluten Free Dietary Supplement *** Manufactured & Distributed by: Magno-Humphries Labs Tigard, OR 97223 U.S.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.

Lot numbers, UPCs & expiration codes

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.

Where it was sold

Distributed to only one consignee with several locations nationwide.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1304-2013
Classification
Class III
Status
Terminated
Recall initiated
Mar 18, 2013
FDA report date
Apr 17, 2013
Quantity
40369 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Magno Humphries Inc

Original FDA data

Every field from FDA enforcement report F-1304-2013, exactly as published.

Show all FDA fields
City
Tigard
State
OR
Status
Terminated
Country
United States
Event ID
64672
Address
8800 Sw Commercial St
Code information
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.
Postal code
97223-6252
Report date
Apr 17, 2013
Product type
Food
Recall number
F-1304-2013
Classification
Class III
Recalling firm
Magno Humphries Inc
Product quantity
40369 bottles
Termination date
Apr 9, 2014
Reason for recall
The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ferrous Sulfate Tablets 325 mg, 100 count bottles, Nutritional Supplement. Label reads in part "OPTIMUM *** FERROUS SULFATE 325 * mg 5 Grain *** Gluten Free Dietary Supplement *** Manufactured & Distributed by: Magno-Humphries Labs Tigard, OR 97223 U.S.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.
Distribution pattern
Distributed to only one consignee with several locations nationwide.
Recall initiation date
Mar 18, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 9, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1304-2013, published Apr 17, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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