immediate action Recalls

2,715 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-1444 Endoscope Air/Water Valve Recall 2026 for 89,579 Units

Olympus Corporation of the Americas is recalling 89,579 MAJ-1444 endoscope air/water valves distributed nationwide in the United States. The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Healthcare facilities should stop using the devices 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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Recalled LSHOME 3-Pack Smoke Detector Fire Alarm packaging
HIGH
CPSC

LShome Smoke Detectors Recalled Over Failure to Warn During Fire

LShome recalled 3-Pack Smoke Detector Fire Alarms on February 12, 2026, due to a failure to warn during a fire. The defect poses a serious risk of injury or death. Consumers should stop using these alarms immediately and contact the manufacturer for a refund.

LShome Photoelectric Smoke Detector Fire Alarms
If the
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Food & Beverages
HIGH
FDA FOOD

Oregon Potato Company Recalls Blueberries Due to Listeria Risk

Oregon Potato Company recalled 55,689 pounds of IQF Blueberries on February 12, 2026, due to potential contamination with Listeria monocytogenes. The affected products include 30-pound cases and 1,400-pound totes distributed in Michigan, Oregon, Washington, Wisconsin, and Canada.

Oregon Potato Company
Listeria monocytogenes
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Health & Personal Care
HIGH
FDA DRUG

Eptifibatide Injection Recalled Over Labeling Error

Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.

EPTIFIBATIDE
Labeling: Not
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Health & Personal Care
HIGH
FDA DEVICE

CareFusion 303 BD Alaris System with Guardrails Suite MX Recall Impacts 1,025,567 Units (2026)

CareFusion 303 recalled 1,025,567 units of the BD Alaris System with Guardrails Suite MX with Point of Care Unit worldwide. The recall concerns labeling that fails to indicate which TLS version must be enabled for secure hospital Wi-Fi communication. Hospitals and clinicians should stop using the device immediately and follow manufacturer instructions. The recall was issued by the FDA and is being

CareFusion 303
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Blockers Recalled for Attenuation Degradation in 51 Units Worldwide (2026)

Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Protective Sleeves Recall: 1,129 Units Worldwide for Attenuation Degradation (202

Burlington Medical recalled 1,129 protective sleeves worldwide after determining attenuation degradation over time. The sleeves were manufactured with Xenolite 800 attenuation material between 2025-01-16 and 2026-01-21. The recall affects products distributed in the United States and internationally. Providers and patients should stop using the sleeve and follow recall instructions from the maker.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Half Aprons Recalled for Attenuation Degradation Risk (2026)

Burlington Medical recalled 402 Half Aprons sold worldwide after potential attenuation degradation. Attenuation material Xenolite 800 may degrade over time, reducing shielding lifespan. Patients and healthcare providers should stop using the aprons immediately and contact Burlington Medical for recall instructions.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Recalled 15,438 Radiation Attenuation Vests Over Degradation Risk (2026)

Burlington Medical recalled 15,438 attenuation vests distributed worldwide after potential attenuation degradation over time. The vests use Xenolite 800 attenuation material and were produced between January 16, 2025 and January 21, 2026. Healthcare providers and patients should stop using the vest immediately and follow recall instructions.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Embrace Shoulder Drill Tower Recalled After Mislabeling; 75 Units in 2026

Waldemar Link GmbH & Co. KG recalled 75 Embrace Shoulder Drill Tower devices distributed to U.S. hospitals after discovering mixed-up article numbers in the device overview. The surgical steps are correct, but the overview labeling is inaccurate. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions sent by email.

Waldemar Link GmbH & Co. KG
The surgical
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical BAT Coverage Recall 1,489 Units Worldwide in 2026

Burlington Medical recalled 1,489 BAT Coverage units worldwide on 2026-02-11 after a design-related issue was identified. The recall targets attenuation material used in the device. The defect could affect the lifespan of the shielding. Healthcare providers and patients should stop using the device and follow manufacturer instructions. The recall is active as of 2026-04-08.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Leg Wraps Recall: 103 Units Worldwide in 2026

Burlington Medical, LLC recalled 103 leg wrap devices distributed worldwide through multiple retailers. The recall cites attenuation degradation over time that could shorten the devices' lifespan. Healthcare providers and patients should stop using them immediately and follow the manufacturer's recall instructions.

Burlington Medical
Potential for
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Tag Statistics

Total Recalls
2,715

Related Tags

stop use immediatelyfda regulatedcpsc regulatedreplacement availablereturn for refundelectronicmetalrepair availableinfant productkitchennhtsa regulatedtip over risk