electrical hazard Recalls

1,030 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed Paradigm Insulin Pumps Recalled 73,656 Units Worldwide in 2026

Medtronic MiniMed recalled 73,656 Paradigm insulin pumps sold worldwide, including broad U.S. distribution, after a risk of unintended insulin delivery. The issue affects Paradigm, 600-series and BLE 700-series pumps. It can cause life-threatening highs or lows in insulin delivery. Stop using the device and follow recall instructions immediately.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)

Olympus Corporation of the Americas recalled 3,354 units of the OER-Pro endoscope reprocessor on February 12, 2026. MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the device 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

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 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

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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Food & Beverages
HIGH
FDA FOOD

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Juniper Granola recalled 1,800 Junebar Chocolate Cherry All Natural Snack Bars sold in New York after undeclared milk and soy were found. The bars carry Lot L1300 and variants L1300A and L1300B. They were produced in a facility that also processes gluten, peanuts, and sesame. Consumers should not eat these bars and should contact Juniper Granola for refunds or replacements.

Juniper Granola
Products contain
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Health & Personal Care
HIGH
FDA DEVICE

Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)

Reflexion Medical recalled 12 RefleXion X1 Radiotherapy System RXM1000 units sold to hospitals and healthcare providers in the United States after a software defect could cause a 5mm or greater misalignment and underdose. The defect occurs during angular roll corrections followed by a repeat localization, and the roll corrections from the initial localization are not carried through to treatment.

Reflexion Medical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Hitachi Proton Beam Therapy Device Recalled for Software Issues

Hitachi Ltd. recalled one unit of its Proton Beam Therapy System on February 6, 2026 due to a software anomaly. The issue may result in positional discrepancies during patient treatment. The recall affects distribution in Texas and Washington D.C.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
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Health & Personal Care
HIGH
FDA DEVICE

Hitachi Proton Beam Therapy System Recalled Due to Software Issue

Hitachi recalled its Proton Beam Therapy System on February 6, 2026, due to a software anomaly that may result in positional discrepancies. The recall affects one unit distributed in Texas and Washington D.C. Healthcare providers and patients must stop using the device immediately.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
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Recalled EnHomee 10 drawer dresser (front)
HIGH
CPSC

EnHomee 10-Drawer Dressers Recalled for Tip-Over Hazard (2026)

EnHomee recalled its 10-Drawer Dressers sold on Amazon after determining tip-over and entrapment hazards. The recall also notes a violation of the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact EnHomee for a full refund.

EnHomee
The recalled
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Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2025 Explorer Over Transmission Valve Issue

Ford Motor Company recalled 2025 Explorers due to transmission valve body issues. The problem may cause unexpected vehicle movement, increasing crash risk. Owners received notification letters on April 11, 2025.

Ford Motor Company
Unexpected vehicle
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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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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

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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Tag Statistics

Total Recalls
1,030

Related Tags

adult productimmediate actionstop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulatedsuffocation riskinfant productnhtsa regulatedholiday productfire hazard