All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

GORE ACUSEAL Vascular Graft Recall Affects 52,306 Devices Worldwide (2025)

Gore recalled 52,306 Gore ACUSEAL Vascular Grafts distributed through healthcare providers in the United States and internationally after reports of graft delamination. Delamination may reduce access flow, cause cannulation difficulties, bleeding or bruising, and may require reinterventions. Healthcare facilities and patients should stop using the device immediately and follow the recall guidance.

Gore
Reports of
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Health & Personal Care
HIGH
FDA DRUG

AvKare Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Foreign Substance Contamination (2025

AvKare recalled 1,512 cartons of CHLORPROMAZINE HYDROCHLORIDE 50 mg tablets distributed nationwide in the U.S. for the presence of a foreign substance. The recall is active as of Sept. 17, 2025. Consumers and healthcare providers should stop using this product immediately and contact AvKARE or a healthcare provider for guidance.

AvKare
Presence of
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Food & Beverages
HIGH
FDA FOOD

Abdallah Candies Recalls Sea Salt Caramel Over Allergen Risk

Abdallah Candies recalled Sea Salt Caramel Dark Miniature on August 25, 2025. The recall affects one 5.20 lb box due to undeclared allergens. Consumers should not consume the product and seek a refund immediately.

Abdallah
Undeclared allergen
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Health & Personal Care
HIGH
FDA DRUG

Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk

Kroger 70% isopropyl alcohol recall active nationwide, 1860 bottles involved. The recall covers Kroger-branded rubbing alcohol distributed by The Kroger Co. No injuries are reported in the notice. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare professional.

Kroger
Cross Contamination
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Vehicles & Parts
HIGH
NHTSA

Kia 2025 K4 and Sorento Recalled for Engine Fasteners SC349

Kia America, Inc. recalls 2025 K4 and Sorento vehicles at Kia dealerships after finding the connecting rod bolts may have been improperly tightened. The defect can cause a loss of drive power, increasing the risk of a crash. Owner notification letters are scheduled to be mailed September 12, 2025, and dealers will replace the sub engine assembly at no charge.

Kia
A loss
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Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft 10-Unit Recall 2025 for Labeling Errors

LeMaitre Vascular recalls 10 Artegraft Collagen Vascular Grafts distributed internationally to Great Britain and Switzerland, with no US distribution. The devices were labeled incorrectly and lacked CE and UKCA marks and missing patient documents. Healthcare providers and patients should stop using the devices and follow recall instructions immediately.

LeMaitre Vascular
Devices were
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.

CooperVision
One lot
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)

CooperVision recalled 180 Softmed Breathables toric daily disposable contact lenses after one lot was manufactured with an invalid sterilization cycle. The lenses were distributed across Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the affected lenses immediately and follow the recall instructions.

CooperVision
One lot
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Vehicles & Parts
HIGH
NHTSA

Ford 2025-2026 F-Series Recalled for Instrument Panel IPC Start-Up Failure (25S88)

Ford is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles because the instrument panel may fail at startup. The recall covers 2025-2026 models. Ford will provide an IPC software update via dealer service or OTA at no cost. Owner letters were mailed September 5, 2025. Contact Ford customer service at 1-866-436-7332. Recall number 25S88.

Ford
An instrument
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Health & Personal Care
HIGH
FDA DRUG

Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected

FDA-listed recall covers 49,275 tubes sold nationwide. Ultra Violette Velvet Screen Blurring Mineral Skinscreen distributed by Grace & Fire USA Inc. Tested SPF results ranged from 4 to 64. Consumers should stop using the product immediately and contact Grace & Fire USA for guidance.

ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN
Subpotent/Super-potent Product:
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Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2025 Explorer and Aviator for Trailer Tail Light Failure (25C42)

Ford recalls 2025 Explorer and Aviator vehicles sold through Ford dealers due to a faulty body control module that can prevent trailer tail lights from illuminating. The defect may reduce visibility for other drivers when towing a trailer. Interim letters alert owners starting Oct 13, 2025, with a final remedy anticipated in April 2026. Ford will perform the repairs at no charge and provide the an

Ford
Trailer tail
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)

GE Medical Systems recalled 29,225 MAC VU360 Acquisition Trunk Cable and Module Holder devices worldwide. The defect can occur when a user inserts the Acquisition Module incorrectly, causing excessive bending and wear of the Acquisition Trunk Cable. A damaged sheath or exposed wires may appear. If a damaged cable is not identified and removed from service, it can overheat. Stop use immediately and

GE Medical Systems
If a
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Health & Personal Care
HIGH
FDA DEVICE

Abbott i-STAT CG8+ Cartridge Recall 2025: 8,962,450 Units

Abbott Point Of Care recalled 8,962,450 i-STAT CG8+ cartridges sold nationwide in the United States. The recall stems from a lack of FDA 510(k) premarket clearance for updated sample types and measurement ranges. Healthcare providers and patients should stop using these cartridges and follow Abbott's recall instructions.

Abbott Point Of Care
Lack of
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