replacement available Recalls

1,215 recalls tagged with “replacement available”.

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

Kia Telluride Exterior Trim Recall for 2023-2025 Models (2027 Recall)

Kia America, Inc. is recalling 2023-2025 Kia Telluride SUVs sold through Kia dealers nationwide after interim notices warned that door belt molding trim can delaminate and detach. A detached trim piece can become a road hazard for other vehicles and increase the risk of a crash. Owners should contact Kia customer service at 800-333-4542 for inspection and repair.

Kia
A detached
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Health & Personal Care
HIGH
FDA DEVICE

Ortoma AB Recalls 261 Inserter Adapters for Hip Cup Tools (2025)

Ortoma AB is recalling 261 Inserter Adapters for the Cup Inserter Tool used in hip replacement procedures sold worldwide, including Florida. The defect is weld breakage between the pin and the inserter holder. Surgeons and patients should stop using the devices immediately and follow the manufacturer's recall instructions.

Ortoma
Due to
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Vehicles & Parts
HIGH
NHTSA

Kia K5 2023-2025 Recall for Loose Rear Window Trim Pieces in 2025

Kia America is recalling 2023-2025 Kia K5 sedans due to loose rear window trim pieces. Left and right rear window trim pieces may loosen and detach, creating a road hazard. Interim notices were mailed September 26, 2025. Dealers will inspect and replace C-pillar trim assemblies free of charge. Owners should contact Kia at 800-333-4542 for guidance.

Kia
Detached trim
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Health & Personal Care
HIGH
FDA DRUG

Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm

Quallent Pharmaceuticals Health LLC recalls 1,856 bottles of Duloxetine delayed-release capsules due to CGMP deviations and an impurity above FDA interim limits. The recall is active as of August 20, 2025. Patients and providers should stop use and contact Breckenridge Pharmaceutical or a healthcare provider for guidance.

DULOXETINE
CGMP Deviations:
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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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Health & Personal Care
HIGH
FDA DEVICE

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Home Health US recalled 4,661 One Step Sterile Lancets for Single Use sold nationwide through Amazon. The recall cites incorrect or missing Unique Device Identifier codes. Consumers should stop using the lancets immediately and follow the recall instructions from Home Health US or their healthcare provider.

Home Health US
Due to
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Recalled FENGQS F7 Pro E-bike
HIGH
CPSC

FENGQS F7 Pro Electric Bikes Recalled for Fire Hazards Sold on Amazon (2025)

FENGQS recalled F7 Pro electric bikes with batteries produced on 2024-04-21. The bikes were sold blue and marketed under the FENGQS name. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Consumers should stop using the recalled bikes immediately and contact FENGQS for a full refund.

FENGQS
The e-bikes'
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Albuterol Sulfate Inhalation Aerosol Recall Expanded for Stability Variance (2025)

Cipla USA Inc. recalls 20,352 packs of Albuterol Sulfate Inhalation Aerosol after failing stability specifications. The defective lots were distributed nationwide in the United States. The issue involves out of specification results in particle size distribution at the 12-month time point. Patients and healthcare providers should stop use and contact Cipla USA for guidance.

Cipla USA Inc.
Failed Stability
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 5 2025 Recall for High Voltage Battery Bus Bar Tightening Short Circuits (2025)

Hyundai Motor America recalls 2025 IONIQ 5 vehicles due to a potentially loose bus bar in the high voltage battery system. The recall covers 2025 IONIQ 5 models. Hyundai says a short circuit could cause a fire. Owners should park outside away from structures until the remedy is complete and contact Hyundai at 1-855-371-9460. The recall number is 280.

Hyundai
An electrical
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Tag Statistics

Total Recalls
1,215

Related Tags

chemical hazardelectrical hazardfda regulatedcpsc regulatedimmediate actionstop use immediatelyreturn for refundinfant producttoddler productadult productelderly productpet related