Health & Personal Care Recalls

1,814 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

Health & Personal Care
HIGH
FDA DRUG

Zydus Icosapent Ethyl Capsules Recalled for Oxidized Ingredient in 60,541 Bottles (2026)

Zydus Pharmaceuticals USA Inc. is recalling 60,541 bottles of Icosapent Ethyl Capsules, 1 g, 120 capsules per bottle, distributed nationwide in the United States. The recall cites oxidized Icosapent Ethyl causing red dots inside capsules and melted capsules. Patients should stop using the medicine immediately and contact Zydus Pharmaceuticals USA Inc. or their clinician for guidance.

ICOSAPENT ETHYL
Failed Tablet/Capsule
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Health & Personal Care
HIGH
FDA DEVICE

Philips Vue Motion V12 Recall for 3,552 Units Over Cine Frame Sequencing Error (2026)

Philips Medical Systems Nederland B.V. recalled 3,552 Vue Motion V12 devices worldwide, including the United States. The recall is due to a potential that mis-ordered frames during dynamic cine runs may display out of sequence. Stop using the device and follow the recall instructions provided by the manufacturer.

Philips Medical Systems Nederland B.V.
Potential that
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Recalled Tomum Minoxidil Hair Regrowth Treatment (Front view)
HIGH
CPSC

Tomum Minoxidil Hair Serum Recalled Over Child Poisoning Risk

Tomum recalled its Minoxidil Hair Growth Treatment on March 5, 2026, due to serious poisoning risks to children. The product lacks required child-resistant packaging, increasing the risk of ingestion. Consumers should stop using the product immediately and contact the company for a safe replacement.

Tomum Minoxidil Hair Serum Spray Bottles
The hair
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Health & Personal Care
HIGH
FDA DEVICE

Koven Technology BiDop 3 Pocket Doppler ES-100V3 Recalled for Fetal Labeling Issue (2026)

Koven Technology recalled 34 BiDop 3 Pocket Dopplers with BT2M20S8C fetal probes nationwide after regulators found the fetal indication on the labeling was not cleared under 510(k). The defect is labeling that misrepresents fetal use. Healthcare providers and patients should stop using the devices and follow recall instructions from the manufacturer.

Koven Technology
Product labeling
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 M20 X-ray System Recall Affects 5,167 Units Worldwide (2026)

Philips Medical Systems Nederland recalled 5,167 Azurion 7 M20 X-ray imaging systems sold to healthcare facilities in the U.S. and internationally. The wired foot switch can fail to initiate imaging or produce intermittent imaging. Hospitals and clinics should stop using the device and follow recall instructions from Philips, with notification by letter to affected parties.

Philips Medical Systems Nederland
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD20 Recall for 5,084 Units Over Intermittent X-ray Imaging (2026)

Philips Medical Systems Nederland B.V. recalled 5,084 ALLURA Xper FD20 imaging systems sold nationwide and internationally after finding that the wired foot switch may fail to initiate X-ray imaging or perform intermittently. The defect can delay or interrupt imaging during patient care. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.

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

Philips ALLURA Xper FD10 OR Table Recalled for Intermittent X-ray Activation (2 Units, 2026)

Philips Medical Systems Nederland B.V. recalls 2 ALLURA Xper FD10 OR Tables after reports that X-ray imaging may not start or may delay when using the wired foot switch. The defect could affect patients during imaging procedures. Healthcare providers should stop using the device and follow recall instructions from the manufacturer.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DRUG

KC Pharmaceuticals Recalled Sterile Eye Drops AC 182,424 Bottles Nationwide (2026)

KC Pharmaceuticals recalled 182,424 Sterile Eye Drops AC bottles sold nationwide under multiple brands including Quality Choice Eye Drops Irritation Relief and Goodsense Ultra Lubricant Eye Drops. The recall cites a lack of assurance of sterility. Consumers should stop using the product immediately and contact KC Pharmaceuticals for guidance.

Quality Choice Eye Drops Irritation Relief
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD10/10 Imaging System Recalled for Intermittent X-ray Activation (112 Units)

Philips recalled 112 ALLURA Xper FD10/10 imaging systems nationwide in the United States and internationally after reports that X-ray imaging may not start or may intermittently stop when using the wired foot switch. The defect affects system codes 722005, 722011, and 722027. Healthcare providers should stop using the devices and follow Philips recall instructions.

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

Philips Azurion 5 M12 X-ray System Recall 2026: 345 Worldwide Units Affected

Philips Medical Systems Nederland B.V. recalled 345 Azurion 5 M12 X-ray systems distributed worldwide after reports that X-ray imaging may not start or may run intermittently when using the wired foot switch. The defect could affect imaging during patient care. Hospitals should stop using the device immediately and follow the recall instructions in the notification letter.

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

Oxoid Microbact 12L Kit 20 Tests Recalled for Misidentification Risk (2026)

Oxoid recalled 2 Microbact 12L Kit 20 Tests MB1128A lot 4494873 distributed nationwide in the United States, including Georgia and California. The kit may identify the wrong organism due to inconclusive color reactions in wells. Laboratories should stop using the kit immediately and follow recall instructions from Oxoid.

Oxoid
Oxoid Ltd.,
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 B20 Interventional X-ray System Recall for 1,523 Units (2026)

Philips Medical Systems Nederland B.V. recalls 1,523 Azurion 7 B20 interventional X-ray systems used by hospitals nationwide after possible failure to initiate X-ray imaging. The defect affects whether imaging starts when using the wired foot switch. Hospitals should stop using the device and follow Philips recall instructions immediately.

Philips
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Biplane OR Table Recall for 4 Units Over Intermittent X-ray Activation (202

Philips Medical Systems Nederland B.V. recalls 4 units of the Allura Xper FD20 Biplane OR Table after identifying intermittent or failed X-ray initiation when using the wired foot switch. The recall covers System Codes 722020 and 722025. Healthcare facilities were notified by letter. Stop using the affected devices and follow Philips instructions.

Philips Medical Systems Nederland
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems in 2026

Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 5 M20 Recall: 920 Imaging Systems Worldwide Affected (2026)

Philips Medical Systems Nederland B.V. recalled 920 Azurion 5 M20 imaging systems worldwide, including 168 in the United States. The recall cites a defect in which X-ray imaging may not start or may begin intermittently when using the wired foot switch. Healthcare providers should stop using the device immediately and await instructions from Philips.

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

Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)

Philips Medical Systems Nederland B.V. recalls 111 Allura Xper FD20/20 imaging systems with System Code 722038. The recall covers 31 units in the United States and 80 abroad. The defect may prevent X-ray imaging from starting or cause intermittent imaging when using the wired foot switch. Stop using the device immediately and follow recall instructions from Philips or your healthcare provider.

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

Philips Allura Xper FD20/15 OR Table Recall for 8 Units Worldwide in 2026

Philips Medical Systems Nederland B.V. recalls 8 Allura Xper FD20/15 OR Tables worldwide due to a risk that X-ray imaging may not start or may stop intermittently when using the wired foot switch. The issue is tied to System Code 722059 and requires immediate action. Hospitals and patients should stop using the device and follow the manufacturer’s recall instructions.

Philips
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Biplane Recalled for Intermittent X-Ray Imaging (2026)

Philips Medical Systems Nederland B.V. recalled 461 Allura Xper FD20 Biplanes sold to healthcare facilities nationwide and internationally. X-ray imaging may not initiate or may occur intermittently when using the wired foot switch. Hospitals should stop using the devices immediately and follow Philips’ recall instructions.

Philips
Philips has
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Health & Personal Care
HIGH
FDA DRUG

KC Pharmaceuticals Sterile Eye Drops Soothing Tears Recall 74,016 Bottles (2026)

KC Pharmaceuticals recalls 74,016 bottles of Sterile Eye Drops Soothing Tears distributed nationwide by Rugby Laboratories and Walgreens. The recall cites a lack of assurance of sterility. Consumers and healthcare providers should stop using the product immediately and contact KC Pharmaceuticals for guidance.

KC Pharmaceuticals
Lack of
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Category Statistics

Total Recalls
1,814
Pages
91
    Health & Personal Care Recalls | RecallRadar