nhtsa regulated Recalls

370 recalls tagged with “nhtsa regulated”.

Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Implant Recall: Endo-Model Replacement Plateau 15-8521/09 Looks to Detach from Screw (

Waldemar Link GmbH & Co. KG recalls 8 units of Endo-Model Replacement Plateau worldwide after a reported risk that a bushing could detach from the screw shaft due to a longitudinal fracture. The recall also covers US distribution in New Jersey. Health authorities have classified the risk as high. Patients and healthcare providers should stop using the device immediately and follow recall guidance.

Waldemar Link GmbH & Co. KG
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model Replacement Plateau Recall for 3 Units Worldwide (2026)

Waldemar Link GmbH & Co. KG recalls its Endo-Model Replacement Plateau implant. Three units are affected worldwide, including New Jersey in the United States. The defect allows a bushing to detach from the screw shaft after a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions. Notification was sent by,

Waldemar Link GmbH & Co. KG
The potential
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Vehicles & Parts
HIGH
NHTSA

Ford 2025 Explorer and Lincoln Aviator Recalled for Rear-View Camera Software Issue (2026)

Ford Motor Company is recalling 2025 Ford Explorer and Lincoln Aviator vehicles due to a rear-view camera image that may fail when the vehicle reaches 10 mph or more. The defect could reduce rear visibility while reversing and raise crash risk. Letters to owners were mailed March 28, 2025, and Ford will provide a free APIM software update via OTA or at a dealer. Recall 24C34.

Ford
The loss
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Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2020-2025 Explorer and Aviator for Second-Row Seat Switch Bezel Issue (25S67)

Ford is recalling certain 2020-2025 Explorer and Aviator SUVs because the easy-entry second-row outer seat switch bezel may bind or stick, causing seats to unlatch, fold, or slide unexpectedly while driving. Dealers will inspect the second-row seat switch and replace the bezel around the switch as necessary, free of charge. Owner notification letters were mailed August 7, 2025; Ford can be reached

Ford
A seat
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Vehicles & Parts
HIGH
NHTSA

Ford 2025 Explorer Recall for Engine Long-Block Defects

Ford is recalling 2025 Explorer SUVs, along with 2025 Transit and F-150 vehicles, due to defects in connecting rods and rod bearings. The issue can cause engine damage and failure. Owner notices were mailed August 15, 2025, and Ford recall number is 25S55. Dealers will inspect and replace the engine long block as needed.

Ford
A damaged
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Vehicles & Parts
HIGH
NHTSA

FORD 2025 F-250 SD Recalled for Brake Pedal Pushrod May Disconnect

Ford Motor Company recalls 2025 F-250 SD and other SD models for a brake pedal pushrod retaining spring that may not be installed. The defect can cause a sudden loss of brake function and a crash risk. Owners should not drive the vehicle until repaired. Ford will inspect and repair the brake pedal assembly free of charge; letters were mailed June 20, 2025.

Ford
A sudden
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Health & Personal Care
LOW
FDA DRUG

Encon Safety Products Recalls AQ 120 GFEW Aquarion Preserved Cartridges in 2026

Encon Safety Products recalls AQ 120 GFEW Aquarion Preserved Cartridges sold nationwide through multiple retailers. The recall cites cGMP deviations in manufacturing. Stop using the product immediately and follow recall guidance from Encon Safety or your healthcare provider.

Encon Safety Products
cGMP deviations.
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Vehicles & Parts
HIGH
NHTSA

Kia Recalled 2025 Sorento Hybrid and 2024-2025 Sorento SUVs for BDC Software Issue

Kia America recalled 2025 Sorento Hybrid and 2024-2025 Sorento SUVs sold at Kia dealerships nationwide after a body domain control software fault may disable low beam headlights and taillights. The defect can reduce visibility and raise crash risk. Owners should contact a Kia dealer for a free software update under recall SC331; notifications were mailed Feb. 21, 2025.

Kia
A loss
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Health & Personal Care
HIGH
FDA DRUG

Sun Pharmaceutical Fluocinolone Acetonide Topical Solution Recall 24,624 Bottles (2025)

Sun Pharmaceutical Industries is recalling 24,624 bottles of Fluocinolone Acetonide Topical Solution nationwide after out-of-spec impurity D was detected. The product is distributed by Taro Pharmaceuticals in the United States and labeled Rx-only. Consumers must stop using the product and consult a healthcare provider for guidance.

Fluocinolone Acetonide
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Vaseline and Other Petroleum Jelly Products for CGMP Violations (2025

Gold Star Distribution is recalling petroleum jelly products nationwide in the United States. The recall covers Vaseline brand products and other jelly variants distributed by Gold Star Distribution. The issue stems from CGMP deviations at the distribution center and insanitary conditions due to rodent exposure. Consumers should stop using the affected products immediately and contact the company.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Intubation Tray Over High Hypoxia Risk

Medline Industries, LP recalled 130 Intubation Trays on December 24, 2025. The recalled trays may contain a smaller suction catheter that could cause respiratory failure. Patients and healthcare providers should stop using the device immediately.

Medline Industries, LP
A smaller
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Health & Personal Care
HIGH
FDA DEVICE

Philips North America Issues Recall for Patient Information Center Software

Philips North America recalled 146 units of Patient Information Center software on December 22, 2025. A software patch modifies Mobile Event Notification filter settings without notifying users. The recall affects units distributed worldwide, including 41 in the U.S.

Philips North America
A recent
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Health & Personal Care
HIGH
FDA DEVICE

Altruan GmbH Clearest Strep-A Cassette Test Recall 188 Units (2025)

Altruan GmbH recalled 188 units of the Clearest Strep-A Cassette Test distributed nationwide in the United States after determining the device was not cleared by the FDA. The test lacks FDA clearance. Healthcare providers and patients should stop using the test immediately and follow the manufacturer’s recall instructions.

Altruan
Product not
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Health & Personal Care
HIGH
FDA DEVICE

Wondfo Streptococcal A At-Home Self-Test Recalled for FDA Clearance Issues (2026)

Wondfo recalled 188 units of Streptococcal A At-Home Self-Test sold nationwide in the United States after regulators found the device was not FDA-cleared. The recall centers on lack of FDA clearance for safety and effectiveness. Consumers should stop using the test immediately and contact Altruan GmbH or their healthcare provider for instructions.

Wondfo
Product not
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 5 2025 Recall for Rear Suspension Bolts Affects Stability Control

Hyundai recalls 2025 IONIQ 5 EVs for improperly tightened rear suspension alignment adjustment bolts. The issue risks loss of stability control and potentially a crash. Hyundai will repair free of charge, with owner notices mailing November 10, 2025. VINs are searchable on NHTSA.gov as of September 13, 2025.

Hyundai
A loss
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 6 Recall Expands for Charging Port Door Detachment

Hyundai Motor America recalls 2023-2025 IONIQ 6 electric vehicles due to a charging port door panel that may detach. Dealers will apply adhesive as the remedy. Owner letters begin November 10, 2025. VINs searchable on NHTSA as of September 13, 2025.

Hyundai
A detached
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Vehicles & Parts
HIGH
NHTSA

Hyundai Palisade 2025 Seat Belt Buckle Recall Affects 2020-2025 Models

Hyundai Motor America recalls 2020-2025 Palisade SUVs sold through Hyundai dealers. The rear and other seat belt buckles may fail to latch. Owner notification letters are scheduled for November 10, 2025, and dealers will inspect and replace buckle assemblies at no cost.

Hyundai
Seat belt
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Tag Statistics

Total Recalls
370

Related Tags

electrical hazardsuffocation riskimmediate actionreturn for refundreplacement availablefederal law violationcpsc regulatedplasticmetalbattery poweredlithium batterystop use immediately