Severity
Moderate
FDA Food recall · Reported February 15, 2023
Raw material tested positive for Cronobacter sakazakii.
Ortho Molecular Products, Inc. recalled Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, packaged under the following b… - a moderate-severity action.
Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, packaged under the following b… was recalled by Ortho Molecular Products, Inc. in February 15, 2023. Reason: Raw material tested positive for Cronobacter sakazakii.. Check the official notice for the remedy. Verify recall #F-0340-2023 with the FDA Food before acting.
The recall
Ortho Molecular Products, Inc. issued this moderate-severity FDA Food recall-Raw material tested positive for Cronobacter sakazakii..
Sourced from official FDA Food enforcement records. Verify recall #F-0340-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0340-2023) was formally reported on February 15, 2023, with the manufacturer initiating the action on January 12, 2023. It is classified under Moderate severity (Class II), with a current status of Terminated. Ortho Molecular Products, Inc. is listed as the recalling firm, operating out of Stevens Point, WI. Federal records list the affected scope as 4,929 bottles.
The documented reason for this recall is: Raw material tested positive for Cronobacter sakazakii. Distribution data in the federal record shows the product reached: Nationwide. Outside the US to Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
4,929 bottles
Related Recalls
6
0 from same agency
Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, packaged under the following brands and sizes. 1. Ortho Molecular Products Fiber Plus, Product #608445, Net Wt. 15.9 oz (450 Grams) UPC 6 15033-00608 2. Ortho Molecular Products, Inc., 3017 Business Park Drive, Stevens Point, WI 54482. 2. Utzy Naturals, Daily Fiber Drink Mix. Net Wt 5.95 oz (168.75 Grams), UPC 8 56420-00632 6. Manufactured for Utzy Naturals, 623 West Main St., Lake Geneva, WI 53147. 3. Ortho Molecular Products Fiber Plus, Product #608445CAN, 450 g, UPC 6 15033-04608 8. Ortho Molecular Products, Inc. 54482 United States. Product is sold in Canada. 4. Ortho Molecular Products Fiber Plus, Product #608445C, Net Wt. 15.9 oz (450 Grams) UPC 6 15033-01608 1. . Ortho Molecular Products, Inc., 3017 Business Park Drive, Stevens Point, WI 54482. Contains CA Prop 65. 5. Unbranded bottled product in 1000cc bottle to be given out by healthcare provider. 608.008J UPC 6 15033 60608 4. 6. Unbranded bottled product in 1000cc bottle to be given out by healthcare provider. 608C.009H UPC 6 15033 61608 3. Contains CA Prop 65.
Raw material tested positive for Cronobacter sakazakii.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0340-2023 |
| Date reported | February 15, 2023 |
| Date initiated | January 12, 2023 |
| Recalling firm | Ortho Molecular Products, Inc. |
| Firm location | Stevens Point, WI |
| Affected scope | 4,929 bottles |
| Distribution | Nationwide. Outside the US to Canada. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported February 15, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.