tip over risk Recalls

243 recalls tagged with “tip over risk”.

Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Convenience Kits Recalled Worldwide Over Rotating Adaptor Unwinding

Medline Industries, LP recalls 20 kits worldwide after post-market surveillance found a risk the syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection with the manifold. The recall affects three Medline SKUs and includes UDI details and lot numbers. Healthcare providers and patients should stop using the device immediately and follow Medline's recall plan

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Olympus PKS Cutting Forceps 920000PK Recalled Worldwide in 2026 for Welding Defects

Olympus recalls 7 PKS Cutting Forceps worldwide because welded components may fail. The devices are used with a 5mm cannula and an electrosurgical generator. Stop using the device and follow the manufacturer’s recall instructions. Healthcare facilities should verify device details and consult Olympus for replacement options.

Olympus Corporation of the Americas
Olympus identified
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Recalled Vive Health Bed Rail Model LVA1024 (front view)
HIGH
CPSC

Vive Health Recalls Bed Rails Due to Entrapment Hazard

Vive Health recalled adult portable bed rails on February 19, 2026, due to serious entrapment risks. The recall affects models LVA1024 and LVA3031BLK. Consumers must stop using the product immediately and contact Vive Health for a full refund.

Ningbo Shenyu Medical Equipment Co., Ltd., of China
The recalled
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Recalled SAMIT Youth Multipurpose Helmet in crack red
HIGH
CPSC

SAMIT Helmets Recalled Due to Serious Head Injury Risk

SAMIT recalled multi-purpose helmets for children on February 19, 2026. The helmets fail to meet safety standards, posing a risk of serious injury or death. Consumers should stop using them immediately and seek a refund.

SAMIT Youth Multi-Purpose Helmets
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Artoura Breast Tissue Expanders Recall for Dull Needle Tips (2026)

Mentor Texas, LP is recalling Artoura Breast Tissue Expanders with infusion sets worldwide, including the United States and Canada. The infusion sets may contain dull or blunt needle tips that are difficult to advance or may break. Patients and healthcare providers should stop using the device and follow recall instructions.

Mentor
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor CPX 4 Breast Tissue Expanders Recalled in 2026 for Dull Needle Tip Hazard

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs on February 18, 2026. Infusion sets may have dull or blunt needle tips that can be difficult to advance or break. Health facilities and patients should stop using the device immediately and follow the recall instructions.

Mentor Texas LP
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medline Industries, LP recalled 14,379 Airway Exam Kits containing Olympus biopsy valves nationwide. The recall cites rubber fragments detaching from the slit of single-use biopsy valves. Potential harm includes a foreign body in the patient’s tracheobronchial tree, inflammatory response, hypoxia, and longer procedures. Providers and patients should stop using the kit and follow recall directions.

Medline Industries, LP
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 720G Insulin Pump Recall 2026 Affects 37,458 Units Worldwide

Medtronic MiniMed recalled 37,458 insulin pumps sold worldwide through healthcare providers, including the MiniMed 720G, after finding that a pump raised above or lowered relative to the infusion site can deliver insulin too much or too little. The defect stems from changes in gravitational force affecting hydrostatic and hydrodynamic pressures at the infusion site. Patients should stop using the

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 620G Insulin Pump Recall Impacts 799 Units Worldwide (2026)

Medtronic MiniMed recalled 799 infusion pumps worldwide, including in the United States. The devices in the Paradigm, 600, and BLE 700 series can deliver too much or too little insulin when their height relative to the infusion site changes due to gravity. Stop using the pump immediately and contact Medtronic MiniMed for instructions on replacement or refund.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed Paradigm Real-Time Insulin Pump Recalled for 29,074 Units Worldwide (2026)

Medtronic MiniMed recalled 29,074 Paradigm Real-Time insulin pumps worldwide. The devices may deliver insulin improperly when the pump is elevated or lowered relative to the infusion site due to gravitational effects. Patients should stop using the pumps immediately and follow recall instructions from the manufacturer and their healthcare provider.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

Olympus Corporation of the Americas recalls 47,383 MAJ-1443 and MAJ-1444 endoscope suction valves distributed nationwide in the United States. The valves are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the valves immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Recalled Beloems Adult Portable Bed Rail – black handles
HIGH
CPSC

Beloems Adult Portable Bed Rails Recalled Over Entrapment Risk

Beloems recalled adult portable bed rails on February 12, 2026, due to serious entrapment and asphyxiation hazards. The recall affects model BL-BR201, which fails to meet mandatory safety standards. Consumers should stop using the product immediately and seek a refund.

Leioujiapin Technology Co., Ltd. dba Beloems, of China
The recalled
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Recalled Fortemotus Adult Portable Bed Rail
HIGH
CPSC

Fortemotus Bed Rails Recalled Over Entrapment and Asphyxiation Risk

Fortemotus Direct recalled adult portable bed rails on February 12, 2026, after discovering serious safety hazards. The bed rails can cause entrapment and asphyxiation, posing a high risk of injury or death. Consumers should stop using the product immediately and seek a full refund.

Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, of China
The recalled
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Recalled SOOWERY 6-Drawer dresser (front)
HIGH
CPSC

SOOWERY 6-Drawer Dressers Recalled Over Tip-Over Hazard

SOOWERY recalled 50,000 6-Drawer Dressers on February 12, 2026, due to tip-over and entrapment hazards. The dressers can cause serious injuries or death if not anchored to the wall. Consumers should stop using the dressers immediately if they are not anchored.

SOOWERY 6-Drawer Dressers
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.

Waldemar Link GmbH & Co. KG
The surgical
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Recalled Fixwal 7- drawer dresser (front)
HIGH
CPSC

Fixwal 7-Drawer Dressers Recalled Over Tip-Over Hazard

Fixwal recalled its 7-Drawer Dressers on February 5, 2026. The dressers pose severe tip-over and entrapment hazards, particularly to children. Consumers should immediately stop using these furniture units and seek a refund.

Fixwal 7-Drawer Dressers
The recalled
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Tag Statistics

Total Recalls
243

Related Tags

electrical hazardchemical hazardsuffocation riskinfant productadult productpet relatedkitchenfederal law violationcpsc regulatedreturn for refundstop use immediatelyreplacement available