2,715 recalls tagged with “immediate action”.
Dorel Home Furnishings recalled Cosco 2-step kitchen steppers on July 31, 2025. The safety bar can detach, posing fall risks. Consumers should stop using the product and seek repairs immediately.
IKEA recalled garlic presses on July 31, 2025, after reports of small metal pieces detaching. The recall affects the IKEA 365+ VÄRDEFULL models with the IKEA logo. Consumers should stop using these products immediately and return them for a refund.
Backyard Kids recalled KidKraft Farm to Table play kitchens on July 31, 2025, after a strangulation hazard was identified. One death has been reported linked to the defect. The recall affects units designed for children ages 3 and older, model number 53411.
Amazon recalled Amazon Basics Premium Foam Eurotop Mattresses on July 31, 2025, due to fire hazards. The mattresses violate federal flammability standards, posing serious risk to consumers. Affected models were sold on Amazon from December 2022 through May 2024.
TTI Consumer Power Tools recalled RIDGID 18Volt Brushless Framing Nailers on July 31, 2025. The recall affects approximately 50,000 units due to a malfunctioning trigger mechanism that poses a laceration hazard. Consumers should stop using these nailers immediately and check for eligibility in the recall.
Tegu recalled its Magnetic Floating Stackers on July 31, 2025, after discovering a magnet ingestion hazard. The recall affects model numbers STA-BGY-801T and STA-BTP-806T. The toys can pose serious injuries or death if magnets detach and are swallowed.
Leatherman recalled Charge Plus and Charge Plus TTi multi-tools on July 31, 2025, due to a laceration hazard. The knife blade tip does not fully fold into the handle, posing a risk of injury. Consumers should stop using the tools immediately and check for recall eligibility.
Medline Industries recalled 7,913 reprocessed AcuNav Ultrasound Catheters on July 31, 2025. The devices may contain harmful residual particulates that pose an infection risk. Patients and healthcare providers should stop using these devices immediately and follow recall instructions.
Medline Industries recalled 7,913 reprocessed electrophysiology catheters on July 31, 2025. The recall affects specific lots that may contain harmful particulates. Using these catheters could lead to serious health risks including embolism or deep vein thrombosis.
Medline Industries recalled 7,913 reprocessed ViewFlex Xtra ICE catheters on July 31, 2025. The recall affects specific lots due to potential residual particulates that may cause serious health risks. Patients and healthcare providers must stop using the devices immediately.
Medline Industries recalled 7,913 electrophysiology catheters on July 31, 2025, due to contamination concerns. Specific lots may contain small residual particulates, posing risks of systemic infection and thrombus formation. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 7,913 reprocessed electrophysiology catheters on July 31, 2025. Residual particulates on patient-contacting surfaces pose a risk of serious infection and thrombus formation. Patients and healthcare providers must stop using these devices immediately.
Contract Medical International GmbH recalled 2,500 Fortress Introducer Sheath Systems on July 30, 2025. Units may have incorrect pouch labeling, leading to potential use of the wrong device version. Patients and healthcare providers should stop using the product immediately.
Exela Pharma Sciences recalled 4.2% Sodium Bicarbonate Injection on July 30, 2025, due to arsenic contamination. The recall affects single-dose vials distributed nationwide. Consumers and healthcare providers must stop using the product immediately.
S.I.N. Implant System Ltda recalled 4,367 dental implants on July 30, 2025, due to improper storage conditions. The recalled products may have compromised packaging, affecting their quality and performance. Patients and healthcare providers should stop using these devices immediately.
Pfizer Inc. recalled 29,004 bottles of Levoxyl on July 29, 2025, due to subpotency. The recall affects levothyroxine sodium tablets, 50 mcg, Rx only, distributed in the U.S. Consumers should stop using the product immediately.
American Health Packaging recalled 26,992 blister packs of Sucralfate Tablets on July 29, 2025. The recall follows CGMP deviations that affect product quality. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Ortho-Clinical Diagnostics recalled 2,320 units of VITROS Chemistry Products LAC Slides on July 29, 2025. Calibration failures in lots from coating 0130 and above delay test results and may impact patient management. Healthcare providers and patients must stop using these slides immediately.
Ortho-Clinical Diagnostics recalled 2,908 units of VITROS Chemistry Products LAC Slides on July 29, 2025. The recall affects lots from coating 0130 and above due to increased calibration failures that delay test results. The issue may impact patient management and was identified through an uptick in customer complaints.
ORTOMA AB recalled 261 Inserter Adapters on July 28, 2025, due to a potential weld failure. The defect poses a risk of improper positioning during hip implant procedures. The recall affects devices distributed worldwide, including the U.S. and countries like Japan and Sweden.