All Product Recalls

Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)

Philips Ultrasound recalled 1 unit of the C9-4 Ultrasound Transducer, Model No. 989605365021, distributed nationwide in the United States. The recall focuses on clarifying and labeling the device’s useful life. Healthcare providers and patients should stop using the device immediately and follow Philips’ instructions for replacement or further steps.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound L17-5 Transducer Recalled for Useful-Life Labeling (2025)

Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recal Size 40 L12-5 Ultrasound Transducers for Labeling Life Span Recall (2026)

Philips recalled 40 L12-5 ultrasound transducers distributed nationwide in the United States after regulators flagged labeling to define the devices' useful life. The recall concerns labeling clarity rather than a device malfunction. Healthcare providers and patients should stop using the device immediately and await instructions from Philips Ultrasound, Inc or their healthcare provider.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound S5-2 Transducer Recall 2025 - 1 Unit Nationwide

Philips Ultrasound recalled 1 unit of the S5-2 Ultrasound Transducer sold nationwide through healthcare distributors. The recall clarifies labeling to define the useful life of the transducer in the field. Healthcare providers should stop using the device and contact Philips Ultrasound for instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 16,898 Units (2025)

Spacelabs Healthcare is recalling 16,898 DVI display cables worldwide, including the United States. The cables are used as external display connectors for certain monitors. The recall follows a risk that inadequately shielded cables may cause electromagnetic interference with other medical devices. Stop using the affected cables immediately and await manufacturer instructions.

Spacelabs Healthcare
Due to
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Recalls 173 CSCS MAS800 Central Station Desktops Over Reboot Risk (2025)

GE Healthcare recalled 173 CSCS MAS800 Central Station desktops distributed worldwide to hospitals after identifying a software fault that can trigger a reboot cycle. The reboot can result in a loss of central patient monitoring. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.

GE Healthcare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound X3-1 Transducer Recalled for Labeling Clarification in 2026 (17 Units)

Philips Ultrasound recalled 17 X3-1 ultrasound transducers nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of transducers in the field. Healthcare providers and patients should stop using the affected devices immediately and await further manufacturer instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DRUG

Endo USA Recalls 1,041 Cartons of Everolimus 5mg Tablets Over IP-C Impurity (2025)

Endo USA, Inc. recalled 1,041 cartons of Everolimus 5mg tablets nationwide in the United States due to an impurity IP-C out of specification. The impurity IP-C is out of specification in the drug product. Patients and healthcare providers should stop using this product immediately and contact Endo USA or their healthcare provider for guidance.

Everolimus
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare CSCS V3 MAS800 Central Station Recalled for 2,306 Units Worldwide (2025)

GE Healthcare recalled 2,306 CSCS V3 MAS800 Central Station desktops worldwide after identifying a software fault that can trigger a continuous reboot cycle. The issue can result in a loss of central monitoring for connected patients. Hospitals should stop using the affected devices and follow the recall instructions from GE HealthCare and Wipro GE Healthcare Private Ltd.

GE Healthcare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 2025 (012-0895-12, 820 Units)

Spacelabs Healthcare has recalled 820 DVI display cables worldwide due to shielding issues that may cause electromagnetic interference with other medical devices. The cables connect monitors used in patient care. Hospitals should stop using the affected cables and follow manufacturer recall instructions. The recall was issued by letter and is active as of 2025.

Spacelabs Healthcare
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound Recalled 11 Mini Multi TEE Transducers Over Useful-Life Labeling (2025)

Philips Ultrasound recalled 11 Mini Multi TEE ultrasound transducers distributed nationwide in the United States after a labeling clarification related to useful life. The recall centers on providing clarification and labeling to define the useful life of transducers in the field. Healthcare providers should stop using the device and follow recall instructions from Philips Ultrasound, Inc or their

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)

Philips Ultrasound recalled 2 units of the Philips OMNI II TEE Ultrasound Transducer sold nationwide through multiple retailers. The recall seeks labeling clarification to define the transducer's useful life. Healthcare facilities should stop using the devices and follow Philips recall instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DRUG

Apotex Ketorolac Tromethamine Ophthalmic Solution Recall 2025: 493,468 Bottles Nationwide

Apotex Corp. is recalling 493,468 bottles of Ketorolac Tromethamine Ophthalmic Solution, 0.5%, Rx Only, sterile, distributed nationwide in the United States. The recall cites lack of assurance of sterility due to improper bottle sealing. Consumers and healthcare providers should stop using the product immediately and contact Apotex Corp. or their healthcare provider for guidance.

Apotex
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems AW Server 2.0, AW Server 3.0, 3.1, 3.2 Recalled For Security Breach Risk (2025)

GE Medical Systems recalled 7,302 AW Server models worldwide, including 1,381 units in the U.S., after identifying a security vulnerability that could expose patient data. The defect could allow a malicious actor to compromise confidentiality, integrity and availability of information. Healthcare providers should stop using the devices immediately and follow manufacturer instructions for recall.

GE Medical Systems
Firm has
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Health & Personal Care
HIGH
FDA DEVICE

Philips X7-2 Ultrasound Transducer Recall for 5 Units Nationwide (2026)

Philips Ultrasound recalled 5 X7-2 ultrasound transducers distributed nationwide to healthcare providers. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare facilities should stop using the recalled devices and follow Philips Ultrasound, Inc instructions or contact their provider for guidance.

Philips Ultrasound
To provide
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Dum Aloo Due to Salmonella Risk

CHETAK NEW YORK recalled over 3.5 million bags of Dum Aloo on September 5, 2025, after testing positive for Salmonella. The recall affects products distributed throughout the United States. Consumers should not eat the product and seek a refund or replacement.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Hot Green Chillies Over Salmonella Risk

Chetak New York recalled over 3.5 million bags of PREMIUM Select Hot Green Chillies on September 5, 2025. The product tested positive for Salmonella, a bacteria that can cause serious illness. Consumers should not eat the product and should seek a refund or replacement immediately.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Falsa Frozen Product Due to Salmonella Risk

CHETAK NEW YORK recalled 3,509,532 bags of PREMIUM Select Falsa KEEP FROZEN on September 5, 2025. The product tested positive for Salmonella, a serious health risk. Consumers should not consume the product and can contact the company for refunds.

CHETAK NEW YORK
Product tested
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