All Product Recalls

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

Recalled KidKraft Farm to Table Play Kitchen
CRITICAL
CPSC

KidKraft Backyard Kids Farm to Table Play Kitchen Recall 2025 After Strangulation Hazard

Backyard Kids recalled KidKraft Farm to Table Play Kitchens in 2025 after one death was reported at multiple retailers. The hazard arises from hooks that hold toy accessories where clothing can snag during climbing or crawling through the back opening. Stop using the play kitchen immediately and contact Backyard Kids for free replacement hooks or repair.

KidKraft
If young
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls 7,913 Reprocessed ViewFlex Xtra ICE Catheters for Particulates (2025 Recall)

Medline Industries, LP is recalling 7,913 reprocessed ViewFlex Xtra ICE Catheters distributed nationwide in the United States. The lots may contain small residual particulates on patient-contacting surfaces. Healthcare providers and patients should stop using the devices immediately and follow recall instructions to obtain replacement or further guidance.

Medline Industries, LP
Specific lots
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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

Medline Livewire Steerable EP Catheters Recalled for Particulates in 2025 (7,913 Units)

Medline recalled 7,913 reprocessed Livewire steerable electrophysiology catheters distributed nationwide in the United States. The devices may contain small residual particulates on patient-contacting surfaces, potentially triggering an inflammatory response or systemic infection. Stop using the device and follow recall instructions from Medline or your healthcare provider.

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

Medline Reprocesses 7,913 Electrophysiology Catheters for Safety Risks

Medline Industries recalled 7,913 reprocessed Inquiry Steerable Diagnostics Catheters due to contamination risks. Some models may contain small residual particulates that can cause severe inflammatory responses or systemic infections. Patients must stop using these devices immediately and contact healthcare providers for further instructions.

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

Over 4,300 S.I.N. Implant EPIKUT Dental Implants Recalled Due to Quality Concerns

S.I.N. Implant System Ltda recalled 4,367 dental implants after reports of potential packaging damage. Improper temperature and storage conditions may compromise product quality and performance. Patients and healthcare providers should stop using these implants immediately and follow the manufacturer's instructions for return.

S.I.N. Implant System Ltda
Dental implants
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Health & Personal Care
HIGH
FDA DEVICE

Ortho-Clinical Diagnostics Recalls 2,320 VITROS LAC Slides for Calibration Failures on XT Systems (W

Ortho-Clinical Diagnostics is recalling 2,320 VITROS LAC Slides nationwide in the United States. The recall affects LAC slides used with VITROS XT 3400 and VITROS XT 7600 analyzers. The issue involves lots coated 0130 and above with Condition Code TH4-63J and can delay lactate tests. Labs should stop using the affected slides and follow manufacturer instructions immediately. Contact Ortho-Clinical

Ortho-Clinical Diagnostics
VITROS Chemistry
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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 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

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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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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Food & Beverages
HIGH
FDA FOOD

Gelson's Hummus Recalled Over Missing Storage Instructions

Gelson's recalled 7,861 units of Red Bell Pepper Hummus on July 25, 2025. Labels failed to include critical storage instructions to keep refrigerated. Consumers should not consume the product and seek refunds.

Gelsons
Gelson branded
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Food & Beverages
HIGH
FDA FOOD

Gelson's Hummus Recalled Over Missing Refrigeration Instructions

Gelson's recalled 7,861 units of its Low Sodium No Cholesterol Classic Hummus on July 25, 2025. The product labels fail to include essential storage instructions to keep refrigerated. Consumers should not consume the product and seek a refund.

Gelsons
Gelson branded
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