Borden Good 2 Gether, UPC: 5300001112, Sharp Cheddar Cheese with Pretzels, Net Wt 2 0z (57 g), Dist. By DFA Dairy Farmers of America, PO ...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2026-2015.
Borden GOOD2GETHER Snack Trays with Sell By dates of 9/16/2015, 9/17/2015, and 9/18/2015 are being recalled by Dairy Farmers of America. The manufacturer of the product trays recently experienced a temporary issue with their equipment, which may have resulted in a hard plastic punch hole knockout measuring 7.91mm being retained in some of the product trays. This has the potential to cause a chokin
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2026-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Dairy Farmers Of America Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2026-2015.
Dairy Farmers OF America Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Dairy Farmers Of America Inc Recall FAQ
Dairy Farmers Of America Inc is the subject of a dairy safety report: Borden Good 2 Gether, UPC: 5300001112, Sharp Cheddar Cheese with Pretzels, Net Wt 2 0z (57 g), Dist. By DFA Dairy Farmers of America, PO .... The notice was published on April 6, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 250 units are potentially affected.