immediate action Recalls

2,679 recalls tagged with “immediate action”.

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

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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Food & Beverages
HIGH
FDA FOOD

Mars Foods Ben's Original Ready Rice Recalled for Stones in 273 Cases (2025)

Mars Foods is recalling 273 cases of Ben's Original Ready Rice Original Long Grain White, 8.8 oz, sold at multiple retailers. The recall cites the possible presence of stones in the product. Consumers should not eat this product and should email Mars Foods for a refund or replacement.

Mars Foods
Possible presence
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies Recalls 11 uCT 760 MD CT Scanners for Cover Interference Risk (2025)

UIH Technologies recalled 11 units of the uCT 760 MD Computed Tomography X-ray System. Third-party outer covers can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals and patients should stop using the device immediately and await manufacturer instructions.

UIH Technologies
Third-party outer
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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 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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Food & Beverages
HIGH
FDA FOOD

M.O.M Enterprises Recalls 46,752 Organic BABY Bedtime Drops Over Yeast Contamination (2025)

M.O.M Enterprises recalled 46,752 bottles of Organic BABY bedtime drops sold nationwide through Unknown retailers after FDA enforcement notice flagged potential yeast contamination. The product is a liquid dietary supplement for infants age 4 months and older. Parents should stop using the product immediately and contact M.O.M Enterprises for refund or replacement.

M.O.M Enterprises
Potential yeast
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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 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 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

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

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

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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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

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

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 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

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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Food & Beverages
HIGH
FDA FOOD

Mars Foods Ben's Original Ready Rice Recall 1,075 Cases Over Stones (2025)

Mars Foods US recalled 1,075 cases of Ben's Original Ready Rice Long Grain & Wild 8.8 oz sold in nine states. The hazard is the possible presence of stones in the product. Consumers should not consume the product and should contact Mars Foods US for refund or replacement by email.

Mars Foods
Possible presence
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Tag Statistics

Total Recalls
2,679

Related Tags

laceration riskstop use immediatelyreplacement availablereturn for refundadult productinfant productelectronicfda regulatedcpsc regulatednhtsa regulatedgarageworkplace