2,756 recalls tagged with “immediate action”.
Canon Medical Systems recalled 22 MRI systems on December 19, 2025, due to a potential ice formation hazard in the venting system. The defect could lead to a pressure build-up and helium gas release. Healthcare providers must stop using the affected devices immediately.
Bisaf Strep A Self-Test from Altruan GmbH remains active in recall status after the FDA flagged lack of clearance. The Class II medical device was distributed nationwide in the United States. The hazard is lack of FDA clearance. Consumers should stop use immediately and follow manufacturer guidance.
Boston Scientific recalled 150 units of its *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System on December 19, 2025. The recall follows increased reports of stent deployment and expansion issues, which could lead to serious medical interventions. Healthcare providers and patients must stop using the device immediately.
Gregory's Foods recalled 308 cases of White Chocolate Macadamia Nut frozen cookie dough on December 19, 2025. The product contains undeclared peanuts, posing a serious allergy risk. Consumers should not consume the product and seek refunds.
Siemens Medical Solutions USA, Inc. recalled 88 units of NAEOTOM Alpha software applications on December 19, 2025. The applications lack FDA 510(k) clearance, posing potential risks to patient safety. Healthcare providers must stop using the software immediately and follow the manufacturer's instructions.
Altruan GmbH recalled 188 units of the Clearest Strep-A Cassette Test distributed nationwide in the United States after determining the device was not cleared by the FDA. The test lacks FDA clearance. Healthcare providers and patients should stop using the test immediately and follow the manufacturer’s recall instructions.
Boston Scientific recalled 588 units of its *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System on December 19, 2025. The recall follows multiple reports of stent deployment and expansion issues, posing serious risks during medical procedures.
Boston Scientific recalled 39 AXIOS Stent and Electrocautery-Enhanced Delivery Systems on December 19, 2025. Reports indicated issues with stent deployment and expansion, potentially leading to additional surgical interventions. The recall affects units distributed worldwide, including the United States and several other countries.
Boston Scientific recalled 59 AXIOS Stents on December 19, 2025. Increased reports of deployment and expansion issues pose serious risks during procedures. Users should stop using the devices immediately and follow recall instructions.
Tyber Medical recalled 100 units of its VOLT Wrist Treatment System on December 19, 2025. The recall stems from a manufacturing defect that affects the thread orientation of anatomical left plates. Healthcare providers and patients should stop using the device immediately.
Rifton Equipment recalled 470 E-Pacer gait training devices on December 18, 2025. The body support strap may fray, posing a risk to users. Health care providers and patients must stop using the device immediately.
Waterfront BISTRO brand Frozen Raw Shrimp was recalled on December 18, 2025, due to possible contamination with Cesium-137. Approximately 1,800 cases of the product are affected. Consumers should not consume the shrimp and seek a refund or replacement.
Rifton Equipment recalled 3,238 TRAM powered lift devices on December 18, 2025, due to a risk of fraying body support straps. This recall affects models K310 sold worldwide, including the US, Europe, and Australia. Healthcare providers and patients must stop using the devices immediately to prevent injury.
CATAO MARKET recalled 520 master cases of its Authentic Cuban Loaf Cake Raisins on December 18, 2025. The recall occurred due to undeclared FD&C Yellow #5, which poses a high allergy risk. The affected products were distributed only in Florida and have best by dates from December 18, 2025, to March 18, 2026.
Meaicezli recalled Play Purse Sets on December 18, 2025, due to a risk of serious injury from battery ingestion. The toys contain button cell and lithium coin batteries accessible to children. Consumers must stop using the products and return them for a full refund.
Blue Wave recalled all above-ground pools 48 inches and taller on December 18, 2025, due to a drowning risk. The pools may allow children to access the water even when ladders are removed. Consumers should stop using these pools immediately and contact Blue Wave for a free repair kit.
Pedego Electric Bikes recalled its Fat Tire Trikes on December 18, 2025, due to fall and laceration hazards. The trikes can develop hairline fractures near the welds, leading to potential accidents. Consumers should stop using the product and contact Pedego for a free repair.
TopHomer recalled pool drain covers on December 18, 2025, due to serious entrapment and drowning hazards. The recall affects 8-inch drain covers sold on Amazon. Consumers should immediately stop using the products and seek refunds.
Imprimis NJOF, LLC recalled 596 boxes of intraocular injections on December 18, 2025. The recall affects products due to the presence of glass-like particles. Consumers should stop using the product immediately and contact their healthcare provider.
Currey & Company recalled all Electra Chandeliers and Electra Three Tier Chandeliers on December 18, 2025 after discovering a ceiling mount defect. This defect could cause the fixtures to fall unexpectedly, posing an impact injury risk. Consumers should stop using these chandeliers immediately and contact the company for repairs.