All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Agilent Technologies Denmark ApS Recalls 67 FLEX CD20 Antibody for Potential Weak Staining

Agilent Technologies Denmark ApS recalled 67 FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use antibodies sold nationwide in the United States. The antibody may stain weakly, potentially producing false negative CD20 results. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.

Agilent Technologies Denmark ApS
Their is
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Health & Personal Care
HIGH
FDA DEVICE

PHILIPS IntelliSpace Cardiovascular Software 8.0.0.4 Recall Affects 4 Units Nationwide

Philips Medical Systems Nederland B.V. recalls four IntelliSpace Cardiovascular software units distributed to facilities in Georgia, North Carolina and Texas. A software issue can display outdated information on the device. Hospitals should stop using the device immediately and follow Philips recall instructions.

Philips Medical Systems Nederland B.V.
Software issue
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025

Baxter Healthcare Corporation issued an urgent medical device recall for one lot of Continu-Flo intravascular solution sets, 14,400 units distributed nationwide in the United States. Customer reports indicate tubing separation. Health care providers and patients should stop using the device immediately and follow recall instructions.

Baxter Healthcare
Baxter Healthcare
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Food & Beverages
HIGH
FDA FOOD

SUNGAL UDK Half Plum 170 g Recall for Cyclamate Adulteration (2025)

SUNGAL Inc. recalls 29 cases of UDK Half Plum, 170 g containers distributed to California, Maryland, New York and Virginia. The product is adulterated with cyclamate. Consumers should not consume it and should email SUNGAL Inc. for refund or replacement information.

SUNGAL
Cyclamate adulteration
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Health & Personal Care
HIGH
FDA DEVICE

Medline Industries Recalls 22 Sterile Convenience Kits DYNJ0382730O, DYNJ61038B (2025)

Medline Industries, LP recalled 22 sterile convenience kits distributed to Florida, Maryland, New Jersey and Tennessee after determining the kits labeled as sterile had not undergone sterilization. The sterility lapse creates an infection risk for patients. Healthcare facilities and patients should stop using the kits and follow the recall instructions from Medline and the FDA.

Medline Industries
Convenience kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Medline Industries recalled 88 units of the Sterile Extremity Pack DYNJ45701B after finding that kits labeled as sterile had not undergone sterilization. The affected distribution covered Florida, Maryland, New Jersey and Tennessee. Hospitals and clinics should stop using the kit immediately and follow Medline's recall instructions.

Medline Industries
Convenience kits
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Health & Personal Care
HIGH
FDA DEVICE

Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units

Schiller, AG recalls 266 Argus PB-3000 vital sign monitors nationwide in the United States. The devices may display an error message during blood pressure measurements when the initial inflation pressure is set high. Authorities urge users to stop using the device and follow manufacturer instructions.

Schiller
Vital sign
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Carvedilol 25 mg Recall for Nitrosamine Impurity Affects 4,800 Bottles (2025)

Glenmark Pharmaceuticals recalls 4,800 bottles of Carvedilol 25 mg tablets distributed nationwide in the USA. The recall cites CGMP deviations and a nitrosamine impurity exceeding the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.

Glenmark Pharmaceuticals
CGMP Deviations:
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Recalled La Ligne Enfant Bonne Nuit Pajamas in Navy with White Trim
HIGH
CPSC

La Ligne Enfant Bonne Nuit Pajamas Recalled for Burn Hazard in 2025

La Ligne recalls Enfant Bonne Nuit children’s pajamas after a burn hazard was identified. The recall covers La Ligne by La Ligne Enfant Bonne Nuit two-piece sets sold in various colors. Consumers should stop using the pajamas and pursue a full refund or store credit.

La Ligne
The recalled
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Recalled Séfralls Minoxidil Hair Generation Serum
CRITICAL
CPSC

Séfralls Minoxidil Hair Generation Serum Recalled for Child Poisoning Risk (2025)

Séfralls Minoxidil Hair Generation Serum, sold by Guangzhou Ariel Biotech, was recalled on August 7, 2025. The serum is packaged in amber dropper bottles with a white and gold dropper and a white, black and gold label. The packaging is not child-resistant, violating the Poison Prevention Packaging Act and creating a poisoning risk for children. Consumers should stop using the serum immediately and

Séfralls
The hair
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Food & Beverages
HIGH
FDA FOOD

Wang Globalnet Recalled 1,705 Frozen Oyster Halves Over Norovirus Risk (2025)

Wang Globalnet recalled 1,705 cases of frozen raw oyster halves sold at 27 retail locations in the Northeast and Southwest. The two lots, B250103 and B250114, are under recall for potential Norovirus contamination. Consumers should not consume these oysters and should contact Wang Globalnet for refunds or replacements.

Wang Globalnet
Oyster product
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Carvedilol Tablets Recalled Over Nitrosamine Impurity

Glenmark Pharmaceuticals Inc. recalls 6,432 bottles of Carvedilol Tablets, USP, 12.5 mg, distributed nationwide in the United States. The recall concerns CGMP deviations and the presence of a nitrosamine impurity above the acceptable intake level. Consumers should stop taking the product and contact Glenmark for guidance.

Glenmark Pharmaceuticals Inc.
CGMP Deviations:
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Recalled TEMI Go Basketball Toy
HIGH
CPSC

TEMI Go Basketball Toy Recalled for Choking Hazard Sold on Amazon (2025)

TEMI Toys recalled the TEMI Go Basketball toy sold on Amazon due to a choking hazard for children under three. The toy stands about 13 inches tall and 4 inches wide and includes three yellow balls. TEMI Toys is offering a full refund to consumers who stop using the product and contact the company.

TEMI Go Basketball Toys
The recalled
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