tip over risk Recalls

67 recalls tagged with “tip over risk”.

Recalled Bellevue Bed Frame
MEDIUM
CPSC

Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames (2026)

Samson International is recalling Bellevue and Oaklynn canopy bed frames sold under the Universal Broadmoor brand. The canopy beams can collapse when the bed is moved, posing an impact and injury risk. Stop using the bed immediately and contact Samson for a free repair kit that includes four mounting brackets and hardware.

Samson International, of High Point, North Carolina
The canopy
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Recalled Aisstxoer Adult Bike Helmet (pink)
HIGH
CPSC

Aisstxoer Adult Bicycle Helmets Recalled Over Head Injury Risk (2026)

Aisstxoer adult bicycle helmets sold on Amazon by YXTDZ Store are being recalled. The helmets fail to meet mandatory safety standards for impact attenuation and stability, creating a serious head-injury risk. Stop using the recalled helmet now and contact YXTDZ Store for a full refund; destroy the helmet and email a photo to yxtdzamz@126.com.

Aisstxoer Adult Bicycle Helmets
The recalled
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Recalled LIVEHOM 11-Drawer Dresser – brown
HIGH
CPSC

LIVEHOM Dressers Recalled Over Tip-Over Hazard Risk

LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.

LIVEHOM 11-Drawer Dressers
The recalled
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Recalled 17 Stories Furniture 14-Drawer Dresser (front)
HIGH
CPSC

17 Stories Furniture Dressers Recalled Over Tip-Over Risk

17 Stories Furniture recalled its 14-drawer dressers on March 12, 2026, due to serious tip-over hazards. The dressers, sold in black, white, and brown, can pose risks of injury or death to children if not anchored. Model numbers include 55SCDR14KDBRDL and 55SCDR14KDCHDL.

Online at Wayfair.com from September 2023 through January 2026 for about $135.
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 5 M12 X-ray System Recall 2026: 345 Worldwide Units Affected

Philips Medical Systems Nederland B.V. recalled 345 Azurion 5 M12 X-ray systems distributed worldwide after reports that X-ray imaging may not start or may run intermittently when using the wired foot switch. The defect could affect imaging during patient care. Hospitals should stop using the device immediately and follow the recall instructions in the notification letter.

Philips Medical Systems Nederland B.V.
Philips has
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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 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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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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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 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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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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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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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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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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Recalled YITA dresser – gray
HIGH
CPSC

YITA Recalls Dressers Due to Serious Tip-Over Hazard

YITA recalled multiple brands of dressers on February 5, 2026, due to a serious tip-over hazard. The dressers can pose risks of injury or death to children if not anchored to the wall. Consumers should stop using the affected models immediately and seek refunds.

YITA
The recalled
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