Health & Personal Care Recalls

1,882 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

Graviti Pharmaceuticals Bupropion Hydrochloride XL 300 mg Recall Impacts 46,512 Bottles (2025)

Graviti Pharmaceuticals Private Limited manufactured Bupropion Hydrochloride Extended-Release Tablets XL 300 mg, distributed nationwide by Rising Pharma Holdings, Inc., in 46,512 bottles. The recall cites failed tablet specifications. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.

Bupropion Hydrochloride
Failed Tablet/Capsule
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Health & Personal Care
HIGH
FDA DEVICE

Alcon CONSTELLATION Ultravit 10K & HyperVit 20K Recall for 28,323 Units (2025)

Alcon recalls 28,323 CONSTELLATION Ultravit 10K and CONSTELLATION HyperVit 20K devices used in hospitals worldwide. The recall lists an unspecified hazard. Hospitals should stop using the devices immediately and follow the manufacturer’s instructions. Access the FDA recall notice for details.

Alcon
XXX
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Health & Personal Care
HIGH
FDA DEVICE

FUJIFILM Healthcare CH-200 Recalled for Broken X-ray Tube Shaft in 16 Units

FUJIFILM Healthcare Americas Corp recalled 16 CH-200 X-ray machines in the domestic market. The shaft that mounts the X-ray tube unit on the support may break. Protective parts may fail when the shaft breaks during frontward lifting. Healthcare providers should stop using the device immediately and follow recall instructions.

FUJIFILM Healthcare
It was
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Health & Personal Care
HIGH
FDA DRUG

Private Label Skin Care Inc. Benzoyl Peroxide 10% Acne Treatment Recalled for Benzene Contamination

A benzoyl peroxide acne treatment sold under mel rx Skin by Private Label Skin Care Inc. is recalled for benzene contamination. The recall covers Lot #58170A and 58172A with expiration date 09/2025 and distribution limited to California and Georgia. Consumers should stop using the product immediately and contact the company for guidance.

Private Label Skin Care
Chemical Contamination:
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Health & Personal Care
HIGH
FDA DRUG

Skin MD Body Acne Cleanser Recalled for Elevated Benzene Levels (2025)

Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser after detecting elevated benzene levels. The recall covers products associated with Lot # 58170A and Lot # 58172A distributed in CA and GA. Consumers should stop use and seek guidance from a healthcare provider.

Skin MD
Chemical Contamination:
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 102 Dual-Head Gamma Cameras for Cardiac Imaging (2025)

GE HealthCare recalled 102 dual-head gamma cameras used for cardiac imaging worldwide after finding that some systems past the End of Guaranteed Service could be moved without adequate detector support. This could place excessive stress on detector mounting mechanisms and may cause a detector to fall, posing life-threatening risk. Hospitals and healthcare providers should stop using the devices IM

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 28 Elscint SPX6 Gamma Cameras Worldwide in 2025

GE HealthCare is recalling 28 Elscint SPX6 dual-head gamma cameras worldwide. The recall cites detectors could be stressed during transport or relocation without adequate detector support, risking a detector fall and life-threatening injury. 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 DRUG

Major Pharmaceuticals Chlorpromazine Hydrochloride 100 mg Recall 2025 — 866 Blister Packs Nationwide

Major Pharmaceuticals recalled 866 Chlorpromazine Hydrochloride 100 mg tablets distributed nationwide after CGMP deviations allowed N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit. The impurity detected raises safety concerns for ongoing use. Stop using the product immediately and contact Harvard Drug Group LLC dba Major Pharmaceuticals or Rugby Laboratories for guidance and,

Major Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Chlorpromazine Hydrochloride 25 mg Tablets Recall 2025 for CGMP Deviations

Major Pharmaceuticals recalled 2,064 blister packs of Chlorpromazine Hydrochloride Tablets, 25 mg, sold nationwide through healthcare providers. The recall follows CGMP deviations that allowed the presence of N-Nitroso Desmethyl Chlorpromazine above the allowed limit. Stop using the product immediately and await guidance from Major Pharmaceuticals or your healthcare provider.

Major Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Elscint Helix Dual-Head Gamma Camera Recall for Detector Fall Risk (3 Units Worldwide,

GE HealthCare Israel, Functional Imaging recalled 3 Elscint Helix dual-head gamma cameras worldwide. If moved without adequate detector support, mounting stress could cause a detector fall and life-threatening injury. Hospitals should stop using the device immediately and contact GE Medical Systems Israel, Functional Imaging for instructions.

GE Healthcare Israel Functional Imaging
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Israel Varicam Gamma Camera Recall: 15 Units Worldwide (2025)

GE Medical Systems Israel recalls 15 Elscint Varicam dual-head gamma cameras worldwide. The recall cites a risk that devices moved without proper detector support, which could cause a detector fall. Clinicians should stop using the devices and follow manufacturer instructions immediately.

GE Medical Systems Israel
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 37 Maxicam Dual-Head Gamma Cameras for Cardiac Imaging (2025)

GE HealthCare Israel recalled 37 Maxicam dual-head gamma cameras distributed worldwide to hospitals. The recall cites potential detector mounting stress if the devices are moved without adequate support. This could result in a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the device and follow recall instructions from GE HealthCare.

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies uEXPLORER MD PET/CT Recall for 2 Units in 2025

UIH Technologies recalled 2 uEXPLORER MD PET/CT systems after finding third-party outer covers can trap between the patient table and gantry. The interference can occur during table movement. Hospitals and healthcare facilities should stop using the devices and await instructions from UIH Technologies LLC.

UIH Technologies
Third-party outer
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Category Statistics

Total Recalls
1,882
Pages
95