243 recalls tagged with “tip over risk”.
Wegmans Food Markets is recalling 521 units of Wegmans Large Ultimate Plain Cheesecake sold in Virginia, Maryland, North Carolina and Washington D.C. The product contains undeclared pecans. Consumers should stop using the product and contact Wegmans for refund or replacement.
Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.
Sunbeam Products recalled more than 1 million Oster French Door Countertop Ovens after reports of doors closing unexpectedly and causing burn risks. The recall covers four Oster models and affects units sold nationwide. Consumers should stop using the ovens and contact Sunbeam for a free repair kit.
Autoez recalls bamboo shades sold on Walmart.com due to high risk of strangulation and entanglement. The shades may have long cords and exposed inner cords. Consumers should stop use immediately and seek a full refund.
Audi and Volkswagen Group of America recall 2025 GTI, Golf R, Audi A5, A6 Sportback E-Tron, S5, S6 Sportback E-Tron, 2026 Q4 Sportback E-Tron and Q4 E-Tron vehicles. The torsion bar in the front seat belt retractors may be damaged during production. Dealers will replace one or both front seat belts at no charge. VIN lookups begin Sept 26, 2025 and owner letters go out Nov 21, 2025.
Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.
Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.
EnHomee recalled Fabric 13-Drawer Dressers sold directly by EnHomee Direct due to a tip-over and entrapment hazard. The units do not meet the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and seek a full refund.
Cardinal Health 200, LLC recalled Salem Sump gastroduodenal tubes worldwide after reports of anti-reflux valve breakage. The ARV can fail under excessive force during use. Healthcare providers and patients should stop using the device immediately and follow the manufacturer instructions for recall communication.
B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.
B BRAUN MEDICAL INC recalls 2,760 units nationwide due to a lid misalignment risk in the catheter connector. The recall covers the PERIFIX FX Continuous Epidural Anesthesia Tray and related components. Healthcare providers should halt use and follow manufacturer instructions for recall remedies.
B Braun Medical recalled 2,450 SESK pain management trays distributed nationwide. The recall cites a potential mispositioned catheter connector lid, classified as Class II with high hazard. Patients and healthcare providers were advised to stop using the device and follow recall instructions.
B BRAUN MEDICAL INC recalls 5,770 PERIFIX FX Epidural Anesthesia Trays nationwide after a potential lid misalignment in the catheter connector. The issue could affect catheter administration. Stop using the device and follow recall instructions immediately. Healthcare providers should contact B Braun for guidance.
Percussionaire recalled 59,160 Phasitron 5 IPV In-Line Valve sets worldwide after an IFU update flagged a pressure-relief leak when used with ventilators. The defect endangers neonates and infants and patients under 10 kg with tidal volumes under 50 mL. Healthcare providers should halt use immediately.
FUJIFILM Healthcare Americas Corp recalled 16 CH-200 X-ray machines in the domestic market. The shaft that mounts the X-ray tube unit on the support may break. Protective parts may fail when the shaft breaks during frontward lifting. Healthcare providers should stop using the device immediately and follow recall instructions.
UIH Technologies recalls 3 units of Shanghai United Imaging Healthcare uMI 780 PET/CT systems after a third-party outer cover can trap between the patient table and gantry. The issue can obstruct table movement. Hospitals are urged to stop using the devices and follow recall instructions.
GE Medical Systems Israel recalls 11 Elscint Cardial dual-head gamma cameras used for cardiac imaging worldwide. The recall concerns detector mounting that could fail if the unit is moved without proper support. Hospitals should stop using these devices immediately and follow GE’s recall instructions.
GE Medical Systems Israel recalls 15 Elscint Varicam dual-head gamma cameras worldwide. The recall cites a risk that devices moved without proper detector support, which could cause a detector fall. Clinicians should stop using the devices and follow manufacturer instructions immediately.
Epoca International recalls Paris Hilton mini beauty fridges sold before August 2024 due to a shorting electrical switch that can overheat and cause a fire. Consumers should stop using the recalled units and seek a full refund. Details and how to claim are on Epoca’s recall page or by phone.