HIGH
CPSC
Furnulem Five-Drawer Dressers Recalled for Tip-Over and Entrapment Risk (2026)
Furnulem
The recalled
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
4,267 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 4,267
- 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
HIGH
HIGH
CPSC
Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Packaging (2026)
Zan International Trading
The essential
Food & Beverages
HIGH
FDA FOOD
IF Holding II Tippy Toes Baby Food Recalled for Patulin Contamination (2026) 1,375 cases
IF Holding II
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
Diagnostica Stago STA Liatest Free Protein S Kit Recalled for 369 Units Worldwide in 2026
The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.
Diagnostica Stago
The potential
HIGH
FDA DEVICE
React Health PHOENIX 5L Oxygen Concentrator
Devices which did not meet internal quality specifications were inadvertently distributed.
3B Medical
Devices which
HIGH
FDA DEVICE
The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.
Potential for the Cassette Loading Lever to break.
Fresenius Kabi USA
Potential for
HIGH
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems Recalled 125 Imactis CT-Navigation System Stereotaxic Accessories in 2026
There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.
GE Medical Systems
There is
Vehicles & Parts
HIGH
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Exactech Equinoxe Ergo 321-09-05 Impactor Handle Recall (120 Units, 2026)
Impactor handle may be missing cross-pin
Exactech
Impactor handle
Health & Personal Care
HIGH
FDA DEVICE
Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)
Ion Beam Applications
It was
Vehicles & Parts
HIGH
NHTSA
Ford recalls 2025 Super Duty F-250 SD, F-350, F-450 for steering column weld defect
Ford Motor Company is recalling 2025 Super Duty F-250, F-350, and F-450 trucks sold through Ford dealers. The steering column shifter may detach due to an improper weld. Owners should stop driving the vehicle and contact a Ford dealer for a free inspection.
Ford
A detached
Food & Beverages
HIGH
FDA FOOD
Pure Solutions Recalls Sleep Formula Over Milk Allergen Risk
Pure Solutions recalled 442 bottles of its sleep supplements on February 3, 2026. The labels did not declare a milk allergen despite containing bovine colostrum. Consumers should stop using the product immediately and seek refunds.
Pure Solutions
Label declares
Health & Personal Care
HIGH
FDA DEVICE
Exactech Equinoxe Core Instrument Kit KIT-311X Recalled for Missing Cross-Pin
Impactor handle may be missing cross-pin
Exactech
Impactor handle
Food & Beverages
HIGH
FDA FOOD
Prime Food Processing Dried Croaker Fish Recalled Over Safety Issues
Prime Food Processing recalled 79 cases of dried croaker fish on February 3, 2026, due to safety concerns. The uneviscerated fish poses a high risk of food poisoning. Consumers should not consume this product and seek refunds.
Prime Food Processing
Uneviscerated Fish
Health & Personal Care
HIGH
FDA DEVICE
B. Braun Medical Recalls BBraun Medical 21G Winged INF 7B3050 for 105,550 Units (2026)
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
B. Braun Medical
The potential
Health & Personal Care
HIGH
FDA DEVICE
B. Braun Medical 21GA Winged Infusion Set 7M2802 Recalled 51,300 Units (2026)
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
B. Braun Medical
The potential
Health & Personal Care
HIGH
FDA DRUG
Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Deviations
Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.
PRO NUMB
cGMP deviations