fda regulated Recalls

689 recalls tagged with “fda regulated”.

Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalls Cucumber Slices Due to Salmonella

PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of Cucumber Peeled Sliced on May 20, 2025. The product may be contaminated with Salmonella, posing a high health risk. Consumers should not consume the product and seek a refund or replacement immediately.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalls Sliced Cucumbers Due to Salmonella

PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of sliced cucumbers on May 20, 2025. The product is contaminated with Salmonella, posing a serious health risk. The recall affects consumers in Virginia, New York, Pennsylvania, and New Jersey.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalls Vegetable Tray Cucumbers Over Salmonella Risk

PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of Vegetable Tray Cucumbers on May 20, 2025. The recall follows contamination with Salmonella, posing a high health risk. The affected products were distributed in Virginia, New York, Pennsylvania, and New Jersey.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

PRIMO No. 1 in Produce Recalls Cucumbers Due to Salmonella Risk

PRIMO No. 1 in Produce recalled 89 cardboard boxes of peeled and diced cucumbers on May 20, 2025. The product may be contaminated with Salmonella, posing a serious health risk. Consumers should not eat these cucumbers and should seek a refund or replacement.

PRIMO No. 1 in Produce
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

Chefs Warehouse Recalls Cucumber Due to Salmonella Risk

Chefs Warehouse recalled 98 cases of cucumbers on May 20, 2025, due to contamination with Salmonella. The recall affects cucumbers distributed in Maryland, Delaware, and Virginia. Consumers should not eat the product and can seek a refund.

Chefs Warehouse
Product is
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Health & Personal Care
HIGH
FDA DEVICE

Surepulse Medical Issues Recall for Newborn Heart Rate Monitor Component

Surepulse Medical recalled the VS Cap Small component of its newborn heart rate monitor on January 20, 2023. The recall stems from incorrect sizing information provided on the product label. This defect poses a significant risk to patient safety.

SUREPULSE MEDICAL
Retroactively reported;
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Health & Personal Care
HIGH
FDA DEVICE

Surepulse Heart Rate Monitor Cap Recalled for Sizing Error

Surepulse Medical recalled the Extra Large VS Cap component of its newborn heart rate monitor on January 20, 2023. The recall followed reports of incorrect sizing information that could impact device use. This recall affects distribution in the U.S., the U.K., the Netherlands, and the United Arab Emirates.

SUREPULSE MEDICAL
Retroactively reported;
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