HIGH
CPSC
Sunnyyes LED Mini Lights Recalled for Battery Ingestion Risk, Despite Reese’s Law Violations
Sunnyyes LED Mini Lights
The recalled
lithium battery Recalls
262 recalls tagged with “lithium battery”.
Health & Personal Care
HIGH
FDA DRUG
ARTIFICIAL TEARS Eye Drops Recalled for Sterility Concerns, 720 Bottles Distributed Nationwide (2026
Lack of Assurance of Sterility
ARTIFICIAL TEARS
Lack of
Health & Personal Care
HIGH
FDA DRUG
Omnipaque Injection Recalled by GE Healthcare for Particulate Matter in 866,570 vials (2026)
OMNIPAQUE
Presence of
Health & Personal Care
HIGH
FDA DRUG
GE Healthcare Omnipaque Iohexol Injection Recall Expanded for Particulate Matter in 306,810 Vials (D
OMNIPAQUE
Presence of
Health & Personal Care
HIGH
FDA DRUG
Clonidine Transdermal System Recall Expanded for CGMP Deviations in 113,943 Cartons (2026)
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.
CLONIDINE TRANSDERMAL SYSTEM
CGMP Deviations:
HIGH
CPSC
Lifetime Brands Recalls BUILT LUUM Light Up Tumblers for Choking and Battery Ingestion Hazards (2026
Lifetime Brands
The recalled
Health & Personal Care
HIGH
FDA DRUG
Teva Octreotide Acetate Injectable Suspension Recall 19,869 Cartons Nationwide (2026)
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
OCTREOTIDE ACETATE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Teva Octreotide Acetate Injectable Suspension Recall Expanded in 2026 for Sterility Concerns
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
OCTREOTIDE ACETATE
Lack of
Vehicles & Parts
HIGH
NHTSA
Honda Recalls 2023-2025 Pilot and 2023-2024 Passport Over Fuel Tank Filler Leakage (2026)
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles. The fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Honda
A fuel
Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Siemens ARTIS pheno and ARTIS Icono Imaging Systems Recalled for Dose-Display Anomaly (2026)
Siemens Medical Solutions USA
During patient
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Wayne Pneumothorax Set Recalled for Expired Shelf Life Labels
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Recall: Strange Bile Duct Stone Exploration Set Labeled with Expired Dates (Z-1784-2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Vehicles & Parts
HIGH
NHTSA
Toyota recalls 2022-2025 Tundra and Tundra Hybrid over reverse light moisture risk
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2022-2025 Toyota Tundra and Tundra Hybrid vehicles. Moisture may enter the reverse light assemblies and cause a light failure.
Toyota Motor Engineering & Manufacturing
Reverse light
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Biplane OR Table Recall for 4 Units Over Intermittent X-ray Activation (202
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems in 2026
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 3 M15 Recall for 798 Units Worldwide Over Intermittent X-ray Imaging (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland
Philips has
Health & Personal Care
HIGH
FDA DRUG
Rising Pharmaceuticals Temozolomide 5 mg Capsules Recall 1,200 Bottles in 2026
Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing
Rising Pharmaceuticals
Failed Impurities/Degradation
Food & Beverages
HIGH
FDA FOOD
CNC Noodle Recall: 427 Cases of Steam Noodles Recalled for Undeclared Wheat (2026)
CNC Noodle
Undeclared wheat.