FDA Warns Top Retailers Over Continued Sale of Recalled Baby Formula

Generated by AI AgentJax MercerReviewed byAInvest News Editorial Team
Monday, Dec 15, 2025 11:15 pm ET2min read
Aime RobotAime Summary

- FDA warns

, , , and for continuing to sell recalled ByHeart infant formula linked to 51 botulism cases.

- Target faced scrutiny for promoting the recalled product with $2 discounts, while retailers failed to provide corrective actions despite repeated FDA requests.

- Legal risks loom as the FDA threatens seizures or injunctions, with analysts monitoring enforcement precedents and corporate accountability measures.

FDA Issues Warnings to Major Retailers Over Baby Formula Recall

The U.S. Food and Drug Administration has issued warning letters to four major retailers for continuing to sell baby formula linked to a nationwide outbreak of infant botulism.

, , , and were all cited for failing to remove the recalled ByHeart infant formula from their shelves. The FDA emphasized that the products had been recalled after being connected to across 19 states.

The health regulator has given the retailers 15 working days to explain how they plan to prevent such violations in the future. Failure to comply could result in legal action, including product seizures or injunctions. The FDA noted that

on the recalled formula in some stores, which it called "an active promotion of a recalled product."

Retailers were also criticized for not providing updated information to the FDA despite multiple follow-ups. In its letter to Target, the agency said it had contacted the company on Nov. 19 to discuss the ineffective recall and asked for a plan to ensure compliance moving forward.

to date.

Why the Standoff Happened

The ByHeart infant formula recall began on Nov. 8 when certain lots were pulled from shelves due to contamination risks. The company expanded the recall to include all of its infant formula products days later. Despite these actions, the formula continued to appear in stores across the country, leading to the FDA's formal warnings

.

The FDA has identified several reasons why the products remained on shelves. Store employees cited confusion over which items were affected by the recall and a lack of awareness. In some cases, the formula was still being promoted for sale, as seen with the $2 discount offered by Target in Arkansas

.

The health regulator has also raised concerns about the retailers' responsiveness to follow-up communication. The FDA sent multiple emails between November and December asking for detailed plans to prevent further sales of the recalled items.

during this time.

How Markets Reacted

The controversy appears to have had mixed effects on the stock market performance of the affected retailers. Target shares rose 0.48% on Monday, reaching $97.56. Walmart's stock also saw a small gain, increasing by 0.08% to $116.79. Kroger and Albertsons did not see immediate movement reported on the day

.

Meanwhile, competitors like Kohl's Corp. and Ulta Beauty saw underperformance on the same day. Kohl's stock dropped 4.68%, while Ulta Beauty fell 1.73%. These mixed results suggest the market is reacting to a range of factors, including broader economic trends and consumer behavior

.

What Analysts Are Watching

The FDA's actions have also drawn attention from legal experts and investors. A law firm has announced an investigation into potential claims against Target, focusing on whether the company's leadership adequately managed risks tied to its marketing strategies

. The firm is representing long-term stockholders who may have been impacted by the fallout from the botulism cases linked to the recalled formula.

Analysts are also watching how the FDA handles enforcement in this case. The possibility of legal action, including product seizures, could set a precedent for future recalls and retailer compliance. The agency's focus on active promotion of recalled items, such as the discounted sales at Target, may signal a stricter approach to holding retailers accountable

.

Additionally, the situation has raised questions about how effectively retailers communicate and implement recall protocols. The FDA's emphasis on corrective actions suggests that it is not enough to merely remove products; companies must also demonstrate proactive steps to prevent future violations

.

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