These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
1,498 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Major Pharmaceuticals recalled 1,394 blister packs of Chlorpromazine Hydrochloride Tablets due to contamination concerns. The recall occurred on September 12, 2025, after the FDA found N-Nitroso Desmethyl Chlorpromazine above acceptable limits. Consumers should stop using these tablets and seek guidance from healthcare providers.
GE HealthCare recalled 45 dual-head nuclear medicine gamma cameras on September 12, 2025. The recall affects devices that may have been relocated without proper support, risking a detector fall. This defect can lead to life-threatening injuries.
GE HealthCare recalled 54 nuclear medicine gamma cameras on September 12, 2025. The recall affects devices that may have been transported without proper detector support. This issue poses a high risk of detector falls, potentially leading to serious injuries.
GE HealthCare recalled 292 nuclear medicine gamma cameras on September 12, 2025. The devices may have been relocated without proper support, risking detector falls. This poses a serious risk of life-threatening injuries.
UIH Technologies recalled two units of the uEXPLORER MD system on September 12, 2025. Third-party covers can trap between the patient table and gantry, causing mechanical interference. Healthcare providers must stop using the device immediately and follow recall instructions.
Ben's Original recalled 273 cases of Ready Rice Original Long Grain White on September 12, 2025. The recall follows concerns about possible stones in the product. Customers in several states, including Texas and California, should not consume the affected rice.
UIH Technologies recalled 3 units of its uMI 780 MD system on September 12, 2025. The device can trap third-party covers, causing table movement interference. Healthcare providers must stop using the device immediately and follow recall instructions.
GE HealthCare recalled 11 Cardial nuclear medicine gamma cameras on September 12, 2025. The recall follows concerns over inadequate detector support potentially leading to life-threatening falls. The affected systems were transported without proper safeguards, compromising safety.
GE HealthCare recalled 205 dual-head nuclear medicine gamma cameras on September 12, 2025. The recall affects models that may have been relocated without proper detector support, leading to potential falls. This issue poses a high risk of life-threatening injury.
Shanghai United Imaging Healthcare Co., Ltd. recalled two units of its uCT 780 MD Computed Tomography X-ray System on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, causing mechanical interference. This recall affects units distributed in the US and internationally.
Shanghai United Imaging Healthcare Co., Ltd. recalled four units of its Positron Emission Tomography and Computed Tomography System on September 12, 2025. The recall stems from a risk of mechanical interference during table movement due to third-party outer covers. Healthcare providers and patients must stop using the device immediately.
GE HealthCare recalled 82 units of the Millenium Myosight gamma camera on September 12, 2025. The recall affects systems that may lack sufficient support during transport, posing a risk of detector falls. This defect can result in life-threatening injuries.
GE HealthCare recalled a dual-head nuclear medicine gamma camera on September 12, 2025, after identifying a risk of detector falls. One unit is affected, posing a high risk of life-threatening injury. Users must stop using the device immediately and follow manufacturer instructions.
Blueroot Health recalled Bariatric Fusion Iron Multivitamins on September 11, 2025, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating federal safety standards. Consumers should stop using the product immediately and seek replacement caps.
Shierdu recalled children's wooden building block cactus toys on September 11, 2025. The toys pose a choking hazard, violating the small parts ban. Consumers should stop using them immediately and seek a refund.
Epoca International recalled Paris Hilton Mini Beauty Fridges on September 11, 2025. The recall affects about 10,000 units due to fire and burn hazards. Consumers should stop using the product immediately and seek a refund.
E&E Foods recalled 925 cases of Goldband Snapper fillets on September 11, 2025, due to mislabeling. Testing confirmed the product was actually Sharptooth Snapper. Consumers should not eat the fish and should seek a refund.
In My Jammers recalled children's button flare pajama sets due to a burn hazard on September 11, 2025. The pajamas violate mandatory flammability standards, posing a risk of injury to children. Consumers should stop using the pajamas immediately and return them for a full refund.
Olympus Corporation of the Americas recalled 1,473 EVIS EXERA II Bronchoscopes on September 11, 2025. The recall addresses critical updates to the instructions for use when combined with laser and coagulation therapies. Healthcare professionals must stop using the device immediately and follow the manufacturer's instructions.
Boston Scientific recalled 172 units of its CXR Preconnect with TENACIO Pump on September 11, 2025. The recall stems from potential inflation and deflation performance issues. The devices were distributed worldwide, including the US and Canada.