Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
GE HealthCare recalled 64 units of the Elscint Model 4XX gamma camera on September 12, 2025. The recall affects systems that lack adequate support during transport, risking detector falls. If the detectors fall, they can cause serious injuries to patients and healthcare providers.
UIH Technologies recalled 95 units of its uMI 550 Positron Emission Tomography and Computed Tomography System on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, posing a mechanical interference risk. Patients and healthcare providers must stop using the device immediately.
Shanghai United Imaging Healthcare Co., Ltd. recalled 11 units of its uCT 760 MD Computed Tomography X-ray System on September 12, 2025. The recall addresses a serious hazard where third-party outer covers can become trapped between the patient table and gantry, leading to mechanical interference. Healthcare providers and patients must stop using the device immediately and follow recall directives
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.
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.
Rising Pharma Holdings recalled 13,440 bottles of Cetirizine Hydrochloride Tablets on September 12, 2025. The tablets are imprinted with incorrect identification. This recall affects consumers nationwide.
Diagnostica Stago recalled 12,740 D-Dimer testing devices on September 12, 2025. The recall follows a risk of underestimating D-Dimer levels in patients. Healthcare providers and patients should stop using the device immediately.
GE HealthCare recalled 28 dual-head gamma cameras on September 12, 2025. The recall comes after concerns that inadequate support during relocation could lead to a detector fall. This situation poses a high risk of life-threatening injury.
MARS FOODS recalled 1,075 cases of Ben's Original Ready Rice Long Grain & Wild on September 12, 2025. The recall stems from a possible presence of stones in the product. Consumers should not consume the affected rice and seek a refund or replacement.
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.
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.
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.
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.
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.
Olympus Corporation of the Americas recalled 3,046 units of its EVIS EXERA III bronchoscope BF-P190 on September 11, 2025. The recall addresses safety concerns regarding the use of the bronchoscope with laser and high-frequency therapy equipment. Healthcare providers must stop using this device immediately.
Olympus Corporation of the Americas recalled 395 units of the EVIS EXERA II Bronchovideoscope BF Type Q180-AC on September 11, 2025. The recall addresses additional instructions for safe use with laser and high-frequency therapy equipment. Healthcare providers must stop using the device immediately.
Boston Scientific recalled the LGX Preconnect with TENACIO Pump on September 11, 2025. The recall affects devices sold in the U.S. and Canada due to inflation and deflation performance issues. Consumers should stop using the device immediately and follow provided instructions.
Tropicana Brands Group recalled 1,599 cases of apple juice on September 11, 2025. A manufacturing deviation may cause spoilage or microbial contamination. The affected juice was distributed in 12 states, including Texas and Colorado.
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.
Olympus Corporation of the Americas recalled 116 units of the BF Type XT40 bronchoscope on September 11, 2025. The recall addresses safety concerns regarding the device's use with laser and high-frequency therapy equipment. Healthcare providers must halt use immediately and follow specific instructions from Olympus.