electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Recalls 122,958 t:slim X2 and Tandem Mobi Pumps Over Autobolus Risk (2025)

Tandem Diabetes Care recalled 122,958 insulin pumps nationwide in the United States, including Puerto Rico. A software defect in versions 7.9.0.1 and 7.10.1 for the t:slim X2 and version 7.9.0.1 for the Tandem Mobi paired with a Dexcom G7 sensor can trigger an unexpected automatic insulin correction bolus, raising the risk of hypoglycemia. Users should stop using the affected devices and follow a)

Tandem Diabetes Care
A software
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Food & Beverages
HIGH
FDA FOOD

Hans Kissle Company Recalls 66 Units of Red Bliss Potato Salad for Undeclared Wheat (2025)

Hans Kissle Company recalled 66 units of Red Bliss Potato Salad distributed in MA, RI, CT, NJ and NY. The recall is due to undeclared wheat and a mislabeling that identifies the product as potato salad while the unit contains pasta salad. Consumers should not eat the product and should contact Hans Kissle Company for refund or replacement via email.

Hans Kissle Company
Contains undeclared
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Health & Personal Care
HIGH
FDA DEVICE

AVID Medical CPT BASIC IR PACK 1646381 Recall for Sterility Risk (2025)

AVID Medical recalls 228 CPT BASIC IR PACKs sold nationwide, including Florida, due to open header bag seals that may compromise sterility. The recall is active as of September 17, 2025. Consumers should stop use and follow manufacturer instructions.

AVID Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

AVID Medical JACK421-04 ENT PACK Recalled for Sterility Risk (2025)

AVID Medical recalled 57 JACK421-04 ENT PACK convenience kits nationwide in Florida. The open header bag seals could compromise sterility. Consumers should stop using the device and follow manufacturer instructions for recall resolution.

AVID Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)

Wasatch Photonics recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.

WASATCH PHOTONICS
Two new
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Health & Personal Care
HIGH
FDA DRUG

Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)

Hospira recalls 49,620 vials of Epinephrine Injection, distributed nationwide in the United States. The recall, active since August 4, 2025, targets vials with NDC 0409-4933-05 and case NDC 0409-4933-10. The hazard is lack of assurance of sterility. Health professionals should stop using the product and contact Pfizer or a healthcare provider for guidance.

Epinephrine
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)

Beckman Coulter has issued a recall for 116 DxC 500 AU Module with ISE and DxC 500i components sold internationally. The recall date is 2025-08-04. A processing fault can cause the Clinical Chemistry test to stay In Progress when an Immunoassay test is run between CC tests. Delays may occur. Stop using the device and contact Beckman Coulter for instructions.

Beckman Coulter
On a
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Recalled Cosco 2-Step Kitchen Stepper model 11349WHG1E
MEDIUM
CPSC

Cosco 2-Step Kitchen Stepper Recall 2025 — 10 Models Affected

Dorel Home Furnishings recalls Cosco 2-Step Kitchen Steppers sold at multiple retailers after reports that the safety bar can detach or break during use. The recall covers 10 model numbers. Consumers should stop using the safety bar immediately and contact Dorel for a free repair kit.

Dorel Home Furnishings
The safety
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Recalled RIDGID 18Volt Brushless 21-Degree Framing Nailer
MEDIUM
CPSC

RIDGID 18V Framing Nailers Recalled for Laceration Hazard (2025)

RIDGID 18V Brushless framing nailers, sold through multiple retailers nationwide, are recalled. The recall covers two models with serial-number ranges CS21146D220001 to CS24165N220001 and CS21275D220001 to CS24165N220001. The dual action engagement system can discharge a nail with the trigger alone, creating a laceration hazard.

RIDGID
The dual
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Recall Reaches 8 Units of LinkSymphoKnee Tibial Components Over Uncoated Screws (2025)

Eight modular LinkSymphoKnee TiNbN tibial components are under recall after production with two uncoated security screws. Waldemar Link GmbH & Co. KG disclosed the issue. The devices were distributed worldwide, including CO, IN, NJ and TX in the United States, plus Germany and Italy. Consumers should stop using the device immediately and follow manufacturer instructions.

Waldemar Link GmbH & Co. KG
Some modular
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalled 7,913 Reprocessed Webster CS Catheters for Electrophysiology Mapping

Medline Industries recalled 7,913 reprocessed Webster CS Catheters for electrophysiology mapping nationwide in the United States. The recall concerns small residual particulates on patient-contacting surfaces that could trigger inflammatory responses or systemic infection. If particulates dislodge and contact circulating blood or the heart, they could cause granulomatous reactions or thrombus, and

Medline Industries, LP
Specific lots
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Health & Personal Care
HIGH
FDA DEVICE

Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R

Fortress Introducer Sheath System recalled 2,500 units linked to label mispackaging. The devices were distributed worldwide, including 15 U.S. states and numerous international markets. The incorrect pouch label lists the 4F version reference and unique device identifier instead of the packaged 6F version. Healthcare providers must stop use and follow manufacturer recall instructions.

Fortress Introducer Sheath System
Units may
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Health & Personal Care
HIGH
FDA DEVICE

Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems

VITROS Chemistry Products LAC Slides recalled after calibration failures on VITROS XT 3400 and VITROS XT 7600 systems. The recall covers catalog 8433880 with 2,908 units distributed nationwide in the US. Manufacturers warn that coating 0130 and above with Condition Code TH4-63J elevates calibration failures, delaying lac test results and potentially impacting patient management. Health providers,病

Ortho-Clinical Diagnostics
VITROS Chemistry
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Vehicles & Parts
HIGH
NHTSA

Ford 2025 Expedition Recalled for Brake Software Issue; OTA Update Available

Ford Motor Company recalls 2025 Expedition and other models over a brake booster software fault. The Electronic Brake Booster module may fail while driving or during ADAS use, reducing power brake assist. Ford will update the module software OTA or via dealer free of charge. Owner notifications started August 22, 2025. Contact Ford at 1-866-436-7332 for details and recall 25S77.

Ford
An unexpected
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Tag Statistics

Total Recalls
1,120

Related Tags

adult productimmediate actionstop use immediatelyreturn for refundfda regulatedreplacement availablesuffocation riskchoking hazardtoddler productinfant productpoisoning riskglass