cpsc regulated Recalls

2,056 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DRUG

Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected

A recall is active for Sucralfate Tablets, USP 1 gram distributed by American Health Packaging. The firm filed for Chapter 11 in September 2024, triggering CGMP deviations and questions about product identity, strength, quality and purity. The recall affects 26,992 blister packs distributed nationwide. Stop using the product and contact Amerisource Health Services or your clinician for guidance.

SUCRALFATE
CGMP Deviations:
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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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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 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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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 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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Health & Personal Care
HIGH
FDA DEVICE

Zap Surgical Systems ZAP-X Radiosurgery System Recalled for 17 Units Worldwide in 2025

Zap Surgical Systems recalled 17 ZAP-X Radiosurgery System units worldwide, including US states FL, CO, NJ, NY and several countries. A software defect could cause the collimator to collide with patient shoulders or the patient table during long gantry moves after proximity errors. Clinicians and patients should stop using the device and follow recall instructions from the manufacturer.

Zap Surgical Systems
If the
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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 Curtis International Minifridge Model EFMIS129 - serial numbers between A2001 to A2308 – except for model numbers containing "EFMIS129-B" or "EFMIS129-C"
HIGH
CPSC

Curtis International Recalls Frigidaire Mini Fridges After Fire Hazard (2025)

Curtis International Ltd. recalled Frigidaire-brand minifridges sold nationwide after more than $700,000 in property damage was reported. Internal electrical components can short circuit and ignite the surrounding plastic housing. Consumers should stop using recalled units immediately and contact Curtis for a full refund.

Frigidaire
The minifridges'
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Recalled HydroTech 5/8-inch x 25-foot Expandable Burst-Proof Hose
MEDIUM
CPSC

Winston Products HydroTech 5/8-Inch Expandable Burst-Proof Hose Recall 2025

Winston Products recalled HydroTech 5/8-inch Expandable Burst-Proof Hoses sold through Home Depot and Walmart. The hoses manufactured on or before August 31, 2024 can burst and create an impact hazard and temporarily impair hearing. Consumers should stop using the hoses immediately and contact Winston Products for a full refund.

Winston Products
The recalled
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Recalled Minecraft Light-Up Slap Ruler Bracelet, Model 718508MCR - Front
HIGH
CPSC

Innovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets (2025)

Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets sold at retailers due to a button cell battery ingestion hazard. The recall covers models 718508MCR and 718075MCR. Consumers should stop using the recalled bracelets immediately and email disposal photos to info@innovativenyc.com to receive a full refund.

Innovative Designs
The battery
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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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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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Tag Statistics

Total Recalls
2,056

Related Tags

adult productchemical hazardstop use immediatelyreturn for refundfederal law violationimmediate actionpoisoning riskliving roombathroomelectrical hazardfda regulatedreplacement available