Health & Personal Care
HIGH
FDA DEVICE
Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)
Beckman Coulter
On a
Recall database
All Product Recalls
Browse 4,420 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
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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
MEDIUM
CPSC
Leatherman Charge Plus Multi-Tools Recalled for Laceration Hazard — Check Your Model
Leatherman
The tip
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
MEDIUM
CPSC
IKEA 365+ VARDEFULL Garlic Press Recalled for Laceration and Ingestion Hazards (2025)
IKEA
Small metal
MEDIUM
MEDIUM
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