CLASS III Food recall · Reported 17 Apr 2013 · FDA Enforcement Report
Ferrous Sulfate Tablets 325 mg, Nutritional Supplement recalled
Magno Humphries is recalling Ferrous Sulfate Tablets 325 mg, Nutritional Supplement, distributed nationwide in the US. The recall was initiated on 18 Mar 2013 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1304-2013
- FDA event ID
- 64672
- Recalling firm
- Magno Humphries, Tigard, OR
- Brand
- Ferrous Sulfate
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 18 Mar 2013
- FDA classified
- 9 Apr 2013
- Reported
- 17 Apr 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Product category
- Dietary Supplements
Timeline
| 18 Mar 2013 | Recall initiated by company | |
| 9 Apr 2013 | Classified by FDA | +22 days |
| 17 Apr 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
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.
Where it was distributed
Distributed to only one consignee with several locations nationwide.
Questions about this recall
Why was it recalled?
The firm found minute pieces of blue material identified by their raw material supplier as polypropylene, a relatively inert plastic.
Which lots are affected?
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 was it sold?
Distributed to only one consignee with several locations nationwide.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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