2,153 recalls tagged with “stop use immediately”.
Tegu recalled two Magnetic Floating Stackers sold at multiple retailers. Models STA-BGY-801T and STA-BTP-806T are affected. The magnets can detach and be ingested, posing a serious injury or death risk. Parents should stop using the toys immediately and contact Tegu for a free replacement.
Dorel Home Furnishings recalls Cosco 2-Step Kitchen Steppers sold at multiple retailers after reports that the safety bar can detach or break during use. The recall covers 10 model numbers. Consumers should stop using the safety bar immediately and contact Dorel for a free repair kit.
IKEA is recalling its 365+ VARDEFULL garlic presses after metal fragments can detach and pose a laceration or ingestion hazard. Consumers should stop using the recalled garlic press immediately and return it to any IKEA store for a full refund. If you cannot return to a store, contact IKEA for disposal instructions to receive the refund.
Amazon recalled Amazon Basics Premium Foam Eurotop Mattresses sold on Amazon. The nine-inch mattresses in twin, full, queen and king sizes were manufactured from 12/22/2022 through 05/16/2024 and violate the federal flammability standard, posing a fire hazard. Stop using the recalled mattress and contact Amazon for a full refund.
Medline Industries recalled 7,913 reprocessed ACUSON AcuNav ultrasound catheters nationwide in the United States. The recall cites residual particulates on patient-contacting surfaces as the hazard. Consumers should stop use and follow manufacturer instructions for recall actions.
Medline Industries, LP is recalling 7,913 reprocessed ViewFlex Xtra ICE Catheters distributed nationwide in the United States. The lots may contain small residual particulates on patient-contacting surfaces. Healthcare providers and patients should stop using the devices immediately and follow recall instructions to obtain replacement or further guidance.
Medline recalled 7,913 reprocessed Livewire steerable electrophysiology catheters distributed nationwide in the United States. The devices may contain small residual particulates on patient-contacting surfaces, potentially triggering an inflammatory response or systemic infection. Stop using the device and follow recall instructions from Medline or your healthcare provider.
Medline Industries recalled 7,913 reprocessed Webster CS Catheters for electrophysiology mapping nationwide in the United States. The recall concerns small residual particulates on patient-contacting surfaces that could trigger inflammatory responses or systemic infection. If particulates dislodge and contact circulating blood or the heart, they could cause granulomatous reactions or thrombus, and
Exela Pharma Sciences recalls 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10 mL, nationwide in the U.S. The recall cites out-of-spec arsenic impurities. Consumers should stop use and contact a healthcare provider. Follow recall notice for guidance and refunds.
Fortress Introducer Sheath System recalled 2,500 units linked to label mispackaging. The devices were distributed worldwide, including 15 U.S. states and numerous international markets. The incorrect pouch label lists the 4F version reference and unique device identifier instead of the packaged 6F version. Healthcare providers must stop use and follow manufacturer recall instructions.
S.I.N. Implant System Ltda recalled 4,367 dental implants after reports of potential packaging damage. Improper temperature and storage conditions may compromise product quality and performance. Patients and healthcare providers should stop using these implants immediately and follow the manufacturer's instructions for return.
A recall is active for Sucralfate Tablets, USP 1 gram distributed by American Health Packaging. The firm filed for Chapter 11 in September 2024, triggering CGMP deviations and questions about product identity, strength, quality and purity. The recall affects 26,992 blister packs distributed nationwide. Stop using the product and contact Amerisource Health Services or your clinician for guidance.
VITROS Chemistry Products LAC Slides recalled after calibration failures on VITROS XT 3400 and VITROS XT 7600 systems. The recall covers catalog 8433880 with 2,908 units distributed nationwide in the US. Manufacturers warn that coating 0130 and above with Condition Code TH4-63J elevates calibration failures, delaying lac test results and potentially impacting patient management. Health providers,病
Ortho-Clinical Diagnostics is recalling 2,320 VITROS LAC Slides nationwide in the United States. The recall affects LAC slides used with VITROS XT 3400 and VITROS XT 7600 analyzers. The issue involves lots coated 0130 and above with Condition Code TH4-63J and can delay lactate tests. Labs should stop using the affected slides and follow manufacturer instructions immediately. Contact Ortho-Clinical
Ortoma AB is recalling 261 Inserter Adapters for the Cup Inserter Tool used in hip replacement procedures sold worldwide, including Florida. The defect is weld breakage between the pin and the inserter holder. Surgeons and patients should stop using the devices immediately and follow the manufacturer's recall instructions.
Kia America, Inc. is recalling 2023-2025 Kia Telluride SUVs sold through Kia dealers nationwide after interim notices warned that door belt molding trim can delaminate and detach. A detached trim piece can become a road hazard for other vehicles and increase the risk of a crash. Owners should contact Kia customer service at 800-333-4542 for inspection and repair.
Dynamic Sports Nutrition recalled 1,566 bottles of WINN-50 vanazolol dietary supplement sold nationwide. The FDA-listed recall cites degradation of an ingredient and sub-potent Vitamin B12. Consumers should stop using the product and contact the company for refunds or replacements.
Kia America is recalling 2023-2025 Kia K5 sedans due to loose rear window trim pieces. Left and right rear window trim pieces may loosen and detach, creating a road hazard. Interim notices were mailed September 26, 2025. Dealers will inspect and replace C-pillar trim assemblies free of charge. Owners should contact Kia at 800-333-4542 for guidance.
Merit Medical Systems recalled 447 10Fore Hemostasis Valves following a manufacturing defect that may cause foreign bodies in the fluid pathway. The silicone quad ring may be deformed or damaged during use, posing serious health risks. Patients and providers should stop using the device immediately and follow recall instructions.
BMW recalls 2025 motorcycles with optional eCall system due to a software error that can deactivate emergency crash notification. OTA or dealer update will fix the issue. Letters to owners go out Sept. 12, 2025. Contact BMW at 1-800-525-7417.