electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalls 489 GEM Premier 5000 PAK Cartridges Over PCSND Errors in Warm-Up

Instrumentation Laboratory recalls 489 GEM Premier 5000 PAK cartridges worldwide after reports of Process Control Solution Not Detected errors during warm-up. iQM2 monitors the testing process and may allow continued use after AutoPAK Validation. The recall highlights potential operational disruptions in patient management.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Overpressure Hazard

Olympus Corporation recalled 744 High Flow Insufflation Units on January 16, 2026. A software algorithm issue may lead to overpressure events during use. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls Medical Dressing Due to Sterility Risk

Integra LifeSciences Corp. recalled 55,276 units of MEDIHONEY Calcium Alginate with Active Leptospermum Honey on January 16, 2026. The recall cites potential packaging failures that may compromise sterility. Affected products include model numbers 31012, 31022, and 31045.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls MediHoney Gel for Packaging Issues

Integra LifeSciences Corp. recalled 49,367 units of MediHoney Gel on January 16, 2026. The recall follows potential packaging failures that may compromise the sterile barrier. Affected products include model numbers 31805 and 31815, distributed worldwide.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Over Software Malfunction

Olympus Corporation recalled 485 units of the High Flow Insufflation Unit, Model UHI-3, on January 16, 2026. The recall follows reports of a software algorithm issue that may cause overpressure events. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Software Hazard

Olympus Corporation recalled 18 High Flow Insufflation Units on January 16, 2026, due to a software issue that can cause overpressure events. The recall affects model number UHI, which is used for laparoscopic procedures. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DEVICE

CVS Wound Care Device Recalled Due to Sterile Barrier Breach

CVS recalled 2,906 units of its wound care device on January 16, 2026. The recall stems from potential packaging failures that may compromise sterility. Affected products include model number CVS405406, distributed across multiple states and internationally.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalled Humeral Socket Insert Over Labeling Issues

Encore Medical, LP recalled 20 units of its RSP Humeral Socket Insert on January 15, 2026. The recall stems from incorrect labeling on knee and humeral socket implants. Patients and healthcare providers should stop using the device immediately.

Encore Medical, LP
Knee and
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Health & Personal Care
HIGH
FDA DEVICE

Aesculap MINOP TROCAR 150MM Recall for 126 Units in 2026

Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.

Aesculap
There is
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Recalled HEZI brand power strip (gray)
HIGH
CPSC

HEZI Power Strips Recalled Over Electrocution Risk

HEZI recalled power strips on January 15, 2026, due to an electrocution hazard. The power strips have an ungrounded metal enclosure that can become energized. Consumers should stop using them immediately and seek a refund.

Dongguan Keben Electrical Appliance Co Ltd, of China
The power
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Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalls EMPOWR 3D Knee Implants Due to Labeling Issues

Encore Medical, LP recalled 14 EMPOWR 3D Knee implants on January 15, 2026. The implants contain incorrect labeling that poses a risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.

Encore Medical, LP
Knee and
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Health & Personal Care
HIGH
FDA DEVICE

Edermy Recalls PIE Trolley System Due to Lack of 510K Clearance

Edermy LLC recalled the PIE Trolley System Model 2005 on January 14, 2026 due to a lack of 510K clearance. The recall affects 27 units distributed nationwide across 15 states. Users must stop using the device and follow the manufacturer's instructions immediately.

Edermy
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Laerdal Medical Recalls Suction Units Over Electromagnetic Noise Hazard

Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.

Laerdal Medical
units manufactured
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Infusion Pump Recalled Due to Incomplete Testing

Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.

Baxter Healthcare
Pumps were
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic Recalls Octopus Nuvo Tissue Stabilizer Due to Assembly Issue

Medtronic recalled two units of the Octopus Nuvo Tissue Stabilizer on January 13, 2026, after identifying an assembly issue. The tubing was incorrectly positioned, posing a high hazard risk to patients. Healthcare providers and patients must stop using the device immediately to prevent potential complications.

Medtronic Perfusion Systems
During the
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model Replacement Plateau Recall for Detachment Risk (2026)

Waldemar Link recalled 1 unit of Endo-Model Replacement Plateau worldwide, including the United States in New Jersey. The device could detach its bushing from the screw shaft because of a longitudinal fracture. Clinicians and patients should stop using the device and await manufacturer instructions.

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

Waldemar Link Endo-Model Replacement Plateau Recalled for Detachment Risk

Waldemar Link GmbH & Co. KG recalled 2 units of Endo-Model Replacement Plateau with Item Number 15-0027/11. The defect could cause the bushing to detach from the screw shaft after a longitudinal fracture. Health care providers and patients should stop using the device and await manufacturer instructions.

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

Waldemar Link Endo-Model 15-0027/12 Implant Recall 2026 for Detachment Risk

Waldemar Link recalled 1 unit of Endo-Model Replacement Plateau implant component distributed worldwide, including New Jersey. The defect involves a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Waldemar Link GmbH & Co. KG
The potential
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Tag Statistics

Total Recalls
1,120

Related Tags

chemical hazardsuffocation riskchoking hazardinfant productadult productteen productpet relatedtoddler productstop use immediatelyreturn for refundreplacement availablefederal law violation
    electrical hazard Recalls | RecallRadar