electrical hazard Recalls

1,046 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe Core Instrument Kit KIT-311X Recalled for Missing Cross-Pin

Exactech recalls 596 Equinoxe Core Instrument Kit units due to a missing cross-pin on the impacter handle. The alert, categorized as a Class II recall, was issued Feb 3, 2026 and remains active. Affected kits were distributed across the United States and in multiple international markets. Stop using the device and follow manufacturer instructions for recall remedies.

Exactech
Impactor handle
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Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Insulin Infusion Pumps Recalled 1,380 Units in 2026 Over Czech Guide Error

Tandem Diabetes Care recalled 1,380 insulin infusion pumps distributed internationally in the Czech Republic and Slovakia after translation errors in the Czech user guide could cause unintended insulin delivery. The most significant error told users to verify the infusion set is connected to the body when it should be confirming it is not connected. Following this instruction could result in a hyp

Tandem Diabetes Care
The Czech
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 780G Recall 2026: 26,851 Pumps Hit Over Software Defects

Medtronic MiniMed recalled 26,851 MiniMed 780G insulin pumps sold worldwide, including the United States and Israel. Three software defects tied to updates 6.60, 6.61, and 6.62 could misdose insulin. Stop using the affected pumps and follow the recall letter for instructions.

Medtronic MiniMed
Three software
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Health & Personal Care
HIGH
FDA DEVICE

Medline Chest Drainage Units Recall Updated IFUs for Adults 18+

Medline Industries recalls 2,894 Aqua-Seal Chest Drainage Units from Cardinal Health after updating IFUs to specify adult patients 18 years and older. The devices were distributed worldwide, including California, Chile and Panama. The update clarifies intended patient population and requires action from healthcare providers to stop use until further notice.

Medline Industries, LP
The instructions
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Violative LuxJet Submersible LED Lights
HIGH
CPSC

LuxJet LED Lights Recalled Due to Battery Ingestion Risk

LuxJet recalled Submersible LED Lights on January 29, 2026, due to ingestion risks from lithium batteries. The recall affects sets of 10 lights sold with multiple batteries. Consumers must stop using the lights and return them for a refund.

LuxJet Submersible LED Lights
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

23,568 Medline Surgical Drapes Recalled Over Infection Risk

Medline Industries recalled 23,568 surgical drapes on January 28, 2026, after reports of fabric delamination during laundering. The delamination may delay patient care and increase the risk of infection. Health care providers and facilities must stop using these drapes immediately and follow the manufacturer's instructions for a remedy.

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

Lutronic CLARITY II Laser System Recalled for 1,525 Units Worldwide in 2026

Lutronic's CLARITY II Laser System, 1,525 units distributed worldwide to US clinics and international markets, is recalled. The devices have reports of sparking and popping during use and may burn patients. Clinics and patients should stop using the device immediately and follow the manufacturer's recall instructions.

Lutronic
Reports of
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Health & Personal Care
HIGH
FDA DEVICE

BD 10 mL Luer-Lok Syringe Recalled Over Bundle Packaging Mix-Up in US; 204,000 Units Affected

BD recalled 204,000 10 mL Luer-Lok/Luer Slip syringes due to a packaging mix-up that placed Luer Slip syringes in a batch designated for Luer Lok syringes. The nationwide recall covers products distributed in California and Texas. Healthcare providers and patients should stop using the affected syringes immediately and consult manufacturer recall instructions.

Becton Dickinson
During the
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 3 M12 Due to Hazard

Philips Medical Systems recalled 291 Azurion 3 M12 systems on January 26, 2026, due to a risk of unexpected table movement. This may occur when the Reset Geometry button is pressed, even if a table lock is active. The recall affects 27 units in the U.S. and 264 units internationally.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 7 B12 Table Due to Safety Risk

Philips Medical Systems Netherlands B.V. recalled 655 Azurion 7 B12 systems on January 26, 2026. The recall affects models 722067, 722225, and 722235 due to unexpected table movement when the Reset Geometry button is pressed. This poses a high risk of injury to patients and healthcare providers.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 5 M12 Over Safety Risk

Philips Medical Systems recalled 326 Azurion 5 M12 systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a risk to patients and healthcare providers. Immediate cessation of use is advised.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 7 B20 System Over Movement Risk

Philips Medical Systems recalled 1,503 Azurion 7 B20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a risk of injury. Healthcare providers must stop using the device and follow recall instructions immediately.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 5 M20 Table Over Movement Hazard

Philips Medical Systems Nederland B.V. recalled 922 Azurion 5 M20 systems on January 26, 2026, due to a defect that causes unexpected table movement. This hazard can occur even with an active table lock when the Reset Geometry button is pressed. The recall includes 101 units in the U.S. and 821 units distributed worldwide.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 7 M12 Due to Hazardous Movement

Philips Medical Systems recalled 1,979 Azurion 7 M12 Systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a high risk of injury. Healthcare providers and patients should stop using the devices immediately.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 7 M20 Over Hazardous Table Movement

Philips Medical Systems recalled 5,136 Azurion 7 M20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a danger to patients and healthcare providers. Consumers should stop using the devices immediately and contact the manufacturer for instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 3 M15 System Due to Hazard

Philips Medical Systems Nederland B.V. recalled 802 Azurion 3 M15 systems on January 26, 2026. The systems may move unexpectedly, posing a risk to patients and healthcare providers. Consumers should stop using the device immediately and follow recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Screw System Recalled for MRI Heating Risk in 5,568 Units (2026)

I.T.S. GmbH has recalled 5,568 units of the I.T.S. Screw System sold nationwide in the United States after MRI safety tests showed higher RF-induced temperature increases under some MRI conditions than the IFU outlined. The defect involves MRI RF heating that could burn patients. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.

I.T.S. GmbH
Updated MRI
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Tag Statistics

Total Recalls
1,046

Related Tags

fabricsuffocation riskinfant productteen productadult productelderly productimmediate actionstop use immediatelyreturn for refundcpsc regulatedfda regulatedmandatory standard violation
    electrical hazard Recalls | RecallRadar