Class IICompletedVoluntary: Firm initiated
Riverside Natural Foods, Ltd.: food recall F-0539-2025
Riverside Natural Foods, Ltd. of North York recalled 1. Mixed Berry Granola Bars; 34oz (40 bars) 2. Mixed Berry Granola Bars; 5.1oz (6 bars) 3. Reason: may contain metal pieces. The FDA listed it as Class II in its Enforcement Report dated Feb 19, 2025; distribution: nationwide.
Record status as published: Completed. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 1. Mixed Berry Granola Bars; 34oz (40 bars) 2. Mixed Berry Granola Bars; 5.1oz (6 bars) 3.
- Product quantity
- 2,408,883 cases
- Reason for recall
- may contain metal pieces
- Codes, lots and dates on the package
- 1. UPC: X002FK87OZ; Best by: 10/04/2025; 11/23/2025; 11/24/2025 and UPC: 10687456216475; best by: 10/04/2025; 11/24/2025 2. UPC: 687456213064 best by: 05/22/2025 up to and including 12/30/2025 and 02/11/2026 and UPC: 00687456215808; best by 07/19/2025; 09/08/2025; 09/16/2025; 01/19/2026
- Distribution pattern
- nationwide
- Recalling firm
- Riverside Natural Foods, Ltd., North York, Canada
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 9, 2024 |
| Classified by the FDA | Feb 11, 2025 |
| Published in the Enforcement Report | Feb 19, 2025 |
Other products in the same recall event
The FDA groups related products under one recall event (event 95906).
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0539-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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