FDA Issues Class I Recall for Lay’s Potato Chips Over Milk Allergen Concern**

Sun Feb 02 2025 18:06:21 GMT+0200 (Eastern European Standard Time)
FDA Issues Class I Recall for Lay’s Potato Chips Over Milk Allergen Concern**

The F.D.A. has heightened the recall status of Lay’s Classic Potato Chips due to undeclared milk, affecting consumers in Oregon and Washington.**


Over 6,000 bags of Lay’s Classic Potato Chips have been recalled due to a serious allergen risk for those sensitive to milk, prompting a Class I recall by the F.D.A. Consumers are advised to check their pantry for affected products.**



The Food and Drug Administration (F.D.A.) has enacted a Class I recall for 6,344 bags of Lay’s Classic Potato Chips, warning of significant risks posed to those with milk allergies or sensitivities. This comes after Frito-Lay, the manufacturer, identified a potential issue with undeclared milk in bags sold in Oregon and Washington.

The initial recall was initiated in December 2024, highlighting concerns surrounding 13-ounce bags of chips. Following rigorous evaluations, the F.D.A. upgraded the recall to its most severe classification, emphasizing that consuming the product could potentially lead to serious health consequences or even fatalities.

Consumers in Oregon and Washington who purchased these bags as early as November 3, 2024, should be particularly cautious. The F.D.A. categorizes recalls into three classes, with Class I representing the highest level of concern. Products with milk, classified as one of the eight primary food allergens, are marked with the “guaranteed fresh” date of February 11, 2025, along with the manufacturing codes 6462307xx or 6463307xx for identification.

Fortunately, there have been no reports linked to allergic reactions directly associated with the recalled bags. Additionally, the F.D.A. has ensured that no other Lay’s products or flavors are impacted by this recall.

The heightened classification of the recall has drawn attention given recent communication limitations put in place by the federal health agency, following changes in its leadership. While further reasoning for this designation hasn’t been disclosed, the agency has paused non-critical public communications as it adjusts its processes.

Consumers are encouraged to stay informed and check their stock to ensure their safety in light of this recall.

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