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 DEVICE

Shanghai United Imaging Healthcare uMI Panorama 35 MD PET/CT System Recalled for 4 Units (2025)

UIH Technologies LLC is recalling 4 Shanghai United Imaging Healthcare uMI Panorama 35 MD PET/CT systems sold in the United States. A third-party outer cover can become trapped between the patient table and gantry during table movement. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions.

Shanghai United Imaging Healthcare
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies uMI 550 MD PET/CT Recalled for 95 Units Over Mechanical Interference Risk (2025)

UIH Technologies LLC recalled 95 uMI 550 MD PET/CT systems sold in the United States after reports that third-party outer covers can become trapped between the patient table and gantry. The covers can interfere with table movement during imaging. Hospitals and clinics should stop using the devices and follow the manufacturer's recall instructions immediately.

UIH Technologies
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies Recalls 8 Shanghai United Imaging uCT 530 MD CT Scanners Over Interference Risk (24

UIH Technologies LLC recalls eight Shanghai United Imaging uCT 530 MD CT scanners sold to U.S. hospitals. Third‑party outer covers can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals should stop using the device immediately and follow recall instructions from UIH Technologies or their healthcare provider.

Shanghai United Imaging Healthcare
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

Shanghai United Imaging Healthcare CT X-ray System uCT 550 MD Recall for 22 Units in 2025

Shanghai United Imaging Healthcare recalled 22 CT X-ray systems, including the uCT 550 MD, sold to healthcare facilities in the United States. A third-party outer cover can become trapped between the patient table and gantry, causing mechanical interference during table movement. Stop using the device and follow the manufacturer’s recall instructions immediately.

Shanghai United Imaging Healthcare
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies Recalls 2 uCT ATLAS MD CT X-ray Systems for Mechanical Interference Risk (2025)

UIH Technologies LLC recalled 2 units of the uCT ATLAS MD CT X-ray System sold to U.S. health care providers after reports of potential mechanical interference during table movement. The issue involves third-party outer covers that can become trapped between the patient table and gantry. Hospitals should stop using the devices immediately and follow recall instructions from UIH Technologies LLC.

UIH Technologies
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Optima NX Recall for Detector Fall Risk (1 Unit)

GE HealthCare recalled 1 Optima NX dual-head gamma camera worldwide after detecting potential detector mounting failure if the unit is moved without proper support. The risk could cause a detector fall and life-threatening injury. Hospitals should stop using the device and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging for guidance.

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

GE HealthCare Millenium MPR Gamma Camera Recalled for 292 Units Worldwide in 2025

GE HealthCare recalled 292 Millenium MPR dual-head gamma cameras worldwide after discovering some units past End of Guaranteed Service may have been transported without adequate detector support. This can place excessive stress on detector mounting and could result in a detector fall with life-threatening injury. Healthcare facilities should stop using the devices immediately and follow recall PIN

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 1,386 Millennium MG/MC Gamma Cameras for Detector Mounting Risk (2025)

GE HealthCare recalled 1,386 Millennium MG/MC dual-head gamma cameras used in cardiac imaging worldwide. The recall notes devices past End of Guaranteed Service may have been transported without adequate detector support, risking mounting failure and possible detector falls. Facilities should stop using the devices and await recall instructions sent by GE Medical Systems Israel, Functional Imaging

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Diagnostica Stago STA Liatest D-Di Recall 12,740 Units Worldwide in 2025

Diagnostica Stago recalled 12,740 STA Liatest D-Di units distributed worldwide after a potential risk of underestimating D-Dimer levels. The two listed lots may produce falsely low results. Stop using the devices immediately and follow recall instructions from Diagnostica Stago or your healthcare provider.

Diagnostica Stago
A potential
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Israel Recalls 11 Elscint Cardial Gamma Cameras in 2025

GE Medical Systems Israel recalls 11 Elscint Cardial dual-head gamma cameras used for cardiac imaging worldwide. The recall concerns detector mounting that could fail if the unit is moved without proper support. Hospitals should stop using these devices immediately and follow GE’s recall instructions.

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

Argon Medical Devices Recalls 1,821 Option Elite IVC Filters for Dilator Resistance Risk (2025)

Argon Medical Devices recalled 1,821 Option Elite Vena Cava Filter System devices sold to U.S. hospitals and international distributors. The recall cites a dilator resistance issue within the introducer sheath that could slow procedures and injure venous tissue. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.

Argon Medical Devices
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Noah Medical Galaxy System GAL-001 Recall of 47 Units for Password-Protected Manual Access (2025)

Noah Medical recalled 47 Galaxy System bronchoscopic visualization devices distributed to 20 US states and internationally to Hong Kong and Australia. The recall centers on password-protected Instructions for Use. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

Noah Medical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls SMV DSXi Nuclear Medicine Gamma Camera (205 Units) for Cardiac Imaging

GE HealthCare recalled 205 SMV DSXi dual-head nuclear medicine gamma cameras used for cardiac imaging distributed worldwide. The recall cites potential detector mounting stress after End of Guaranteed Service. Hospitals should stop using these devices and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging or a healthcare provider for guidance.

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Recalls 82 Millenium Myosight Dual-Head Gamma Cameras for Cardiac Imaging (2025)

GE HealthCare recalled 82 Millenium Myosight dual-head gamma cameras distributed worldwide. The devices could have been moved without adequate detector mounting support. This could cause a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the cameras immediately and follow manufacturer recall instructions.

GE Healthcare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 64 Elscint Model 4XX Gamma Cameras in 2025

GE HealthCare recalls 64 Elscint Model 4XX dual-head gamma cameras used for cardiac imaging worldwide after discovering potential detector mounting failure during transport. A detector fall could cause life-threatening injuries. Hospitals should stop using the device and follow the manufacturer’s recall instructions.

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DRUG

Unique Pharmaceuticals Cetirizine Hydrochloride 10 mg Tablets Recalled Nationwide in 2025

9,936 bottles of Cetirizine Hydrochloride Tablets USP 10 mg were recalled nationwide in the United States. Manufactured by Unique Pharmaceuticals Labs and distributed by Rising Pharma Holdings, the lot carries imprint with the wrong ID. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.

Cetirizine Hydrochloride
Tablet/Capsules Imprinted
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Israel Recalls Elscint SPX4 Gamma Camera for Cardiac Imaging

GE Medical Systems Israel is recalling 45 units of the Elscint SPX4 dual-head gamma camera worldwide. The recall cites a risk from transporting or relocating systems past End of Guaranteed Service without adequate detector support. Hospitals and clinics should stop using the device immediately and follow manufacturer instructions.

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

UIH Technologies uCT 780 MD CT Scanner Recalled for Cover Interference (2025)

UIH Technologies recalled 2 units of the uCT 780 MD computed tomography system after an FDA enforcement notice Z-0220-2026. A third-party outer cover can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals should stop using the device immediately and await instructions from UIH Technologies LLC or their healthcare provider.

UIH Technologies
Third-party outer
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Category Statistics

Total Recalls
1,882
Pages
95