Food & Beverages
HIGH
FDA FOOD
DFA Dairy Brands Frozen Dessert Recalled for Undeclared Wheat and Soy, 324 Containers Affected
Product contains undeclared wheat and soy.
DFA Dairy Brands
Product contains
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
3,585 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 3,585
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Health & Personal Care
HIGH
FDA DEVICE
Waldemar Link Recall Reaches 8 Units of LinkSymphoKnee Tibial Components Over Uncoated Screws (2025)
Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.
Waldemar Link GmbH & Co. KG
Some modular
HIGH
HIGH
CPSC
Amazon Recalls Amazon Basics Premium Foam Eurotop Mattress for Fire Hazard (2025)
Amazon
The recalled
HIGH
CRITICAL
CPSC
KidKraft Backyard Kids Farm to Table Play Kitchen Recall 2025 After Strangulation Hazard
KidKraft
If young
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls 7,913 Reprocessed ViewFlex Xtra ICE Catheters for Particulates (2025 Recall)
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalled 7,913 Reprocessed ACUSON AcuNav Ultrasound Catheters for Intracardiac Imaging
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalled 7,913 Reprocessed Webster CS Catheters for Electrophysiology Mapping
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Medline Livewire Steerable EP Catheters Recalled for Particulates in 2025 (7,913 Units)
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Medline Reprocesses 7,913 Electrophysiology Catheters for Safety Risks
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R
Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.
Fortress Introducer Sheath System
Units may
Health & Personal Care
HIGH
FDA DRUG
Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec
Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.
SODIUM BICARBONATE
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
Over 4,300 S.I.N. Implant EPIKUT Dental Implants Recalled Due to Quality Concerns
Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance.
S.I.N. Implant System Ltda
Dental implants
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
VITROS Chemistry
Health & Personal Care
HIGH
FDA DRUG
Pfizer Levoxyl Recall: Subpotent Levoxyl 50 mcg Tablets, 29,004 Bottles in U.S. Market (2025)
Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.
Levoxyl
Subpotent drug
Health & Personal Care
HIGH
FDA DEVICE
Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems
Ortho-Clinical Diagnostics
VITROS Chemistry
Health & Personal Care
HIGH
FDA DRUG
Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected
SUCRALFATE
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Ortoma AB Recalls 261 Inserter Adapters for Hip Cup Tools (2025)
Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.
Ortoma
Due to
Vehicles & Parts
HIGH
NHTSA
Kia K5 2023-2025 Recall for Loose Rear Window Trim Pieces in 2025
Kia America, Inc. (Kia) is recalling certain 2023-2025 K5 vehicles. The left and right rear window trim pieces may loosen and detach.
Kia
Detached trim