Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,021 found- Stop using nowConsumer product
Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
CVS Health recalls medicated hemorrhoidal wipes due to non-child-resistant packaging, risking serious injury or death from child poisoning. Consumers must secure wipes out of reach and return unopened packets for refund.
Diamond WipesJul 2, 2026 - Stop using nowConsumer product
Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fire Hazard
Cooper Lighting recalls Metalux Optimized High Bay LED fixtures due to fire risk from overheating boards. Stop using immediately and contact for free repair or replacement.
Cooper LightingJul 2, 2026 - Stop using nowConsumer product
Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard
Conair recalls over 1 million metal wire grill brushes due to small metal bristles that can detach and cause serious internal injuries requiring surgery.
ConairJul 2, 2026 - Stop using nowConsumer product
AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions; Sold on Amazon by Pretty-Life
AMASKY Nursing Pillows (models BXP99-BXP97) sold on Amazon by Pretty-Life are recalled due to suffocation risk. Consumers must stop using immediately and return for refund.
AMASKYJul 2, 2026 - Use cautionVehicle
RAM 1500 (2026) recall — Exterior Lighting
Chrysler recalls 2026 Ram 1500 vehicles with faulty headlight wiring that causes parking and daytime running lights to flicker or fail, increasing crash risk. Owners must have headlight assemblies inspected and replaced free by dealers.
ChryslerJul 1, 2026 - Lower riskMedical device
Philips North America Llc recalls Cardiac Workstation 5000. Product Number: 860439.
Philips recalls Cardiac Workstation 5000 (product number 860439) due to potential inaccurate native heart rate data. Affected units include specific serial numbers listed in the recall.
PhilipsJul 1, 2026 - Stop using nowDrug
Victory Medical Center Pharmacy recalls Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol
Victory Medical Center Pharmacy recalls Glutathione vials (200 mg/mL, 30 mL) due to bacterial endotoxin contamination. Affected lots: 1984345, 1980571, 1981940. Use before date 08/27/2026.
Victory Medical Center PharmacyJul 1, 2026 - Lower riskMedical device
Aniara Diagnostica LLC recalls 5-PLASMA Bivalirudin Control, Model Number 5D-44905
Aniara Diagnostica recalls 5-PLASMA Bivalirudin Control (Model 5D-44905) due to stability issues causing degraded bivalirudin measurements. Affected units have UDI-DI: 05070002420385 and Lot Number KE132602.
Aniara DiagnosticaJul 1, 2026 - Lower riskMedical device
Biomet, Inc. recalls Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade
Biomet recalls Intramedullary Bone Saw Blade Assembly Model 475625 due to potential sterile packaging damage from exposed blades. Affected units may pose infection risks during surgery.
BiometJul 1, 2026 - Use cautionFood
JINA F&C recalls Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169
JINA F&C recalls Ultimate Mother's Day Wangshin Doenjang because the label fails to list anchovy (fish) as an allergen, posing a risk to those with fish allergies.
JINA F&CJul 1, 2026 - Lower riskFood
Eunha Fisheries Co., LTD recalls FLOUNDER SASHIMI WITH SAUCE; Keep Frozen; Net WT: 300g; UPC: 8 809342 366186
Eunha Fisheries recalls frozen flounder sashimi with undeclared allergens like wheat, soy, sesame, and food dyes. Consumers should check UPC 8 809342 366186 for affected products.
Eunha FisheriesJul 1, 2026 - Use cautionMedical device
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 40mm (Catalog 50796040) due to potential cracking after cleaning and sterilization. Affected units may require replacement.
StrykerJul 1, 2026 - Use cautionFood
Mellish Island Corp recalls Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792
Mellish Island Corp recalls Super Skin dietary supplements because the label fails to declare fish as the source of marine collagen.
Mellish IslandJul 1, 2026 - Use cautionVehicle
NISSAN ROGUE (2026) recall — Power Train
Nissan is recalling certain 2026 Rogue vehicles due to a missing gear selection indicator that may cause unintended vehicle movement or rollaway, increasing crash risk. Owners must contact Nissan for free transmission control valve replacement.
NissanJul 1, 2026 - Use cautionVehicle
BMW I5 (2025) recall — Service Brakes, Hydraulic
BMW recalls certain 2024-2025 I5 vehicles for potential brake system failure that could increase crash risk. Owners must have brake system inspected by August 21, 2026.
BMWJul 1, 2026 - UnratedMedical device
Maquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system,
Getinge recalls SERVO-U/N ventilator sensor modules (model 6693662) due to untested electrical and functional safety during production. Affected units have specific serial numbers. Consumers should contact Getinge for details.
GetingeJun 30, 2026 - Use cautionMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.
Recall of Fresenius Medical Care 2008T BlueStar Hemodialysis Machines with model numbers 191126 and 191130 due to flow, no water, or temperature-related alarms.
Fresenius Medical CareJun 30, 2026 - Lower riskMedical device
restor3d Inc. recalls Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog
restor3d recalls Veritas Standard Glenoid Baseplate models 1500-1030 and 1500-1035 due to potential improper screw engagement. Affected patients should contact the manufacturer for details.
restor3dJun 30, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Baxter recalls Duo-Vent Solution Sets with air bubbles in drip chamber when pressure cuff is used or tubing flushed fully open. Affected units have specific product codes and expiration dates.
BaxterJun 30, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
Medline recalls 150-count germicidal bleach wipes that may have reduced bleach concentration, risking less effective disinfection. Affected items sold between May 2025 and April 2026.
MedlineJun 30, 2026 - Lower riskMedical device
Merge Healthcare, Inc. recalls Merge PACS, medical imaging diagnostic workstation
Merge Healthcare recalls medical imaging workstations where thumbnails from opened patient studies may display incorrectly. Affected versions include 9.4, 9.4 P01, and :9.4 P02. No immediate action needed.
Merge HealthcareJun 30, 2026 - Lower riskMedical device
Boston Scientific Corporation recalls Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 LC 240cm Box 20;
Boston Scientific recalls Radial Jaw 4 Large Capacity Biopsy Forceps with potential packaging breaches that could compromise sterility during medical procedures. Affected units include specific box sizes and lot numbers.
Boston ScientificJun 30, 2026 - UnratedDrug
Ascend Laboratories, LLC recalls Dabigatran etexilate Capsules, 150 mg, 20-count carton (2x10), Rx only, Manufactured by: Alkem Laboratories, Mumbai,
Ascend Laboratories recalls 150mg Dabigatran etexilate capsules (NDC 0904-7255-10) manufactured by Alkem Laboratories in India. The capsules failed impurity tests during stability testing, potentially posing health risks.
Ascend LaboratoriesJun 30, 2026 - Use cautionVehicle
JEEP GRAND WAGONEER (2026) recall — Electronic Stability Control (Esc)
Chrysler recalls 2026 Jeep Grand Wagoneer models with potential loss of electronic stability control and brake assist. Owners must update software by July 30, 2026 to prevent crash risks.
ChryslerJun 30, 2026 - Lower riskMedical device
KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
KENT IMAGING recalls SnapshotGLO Wound Imaging Device models KB100 and KB100AA due to battery charging software issues that cause temporary unavailability after full discharge.
KENT IMAGINGJun 30, 2026 - Use cautionVehicle
FORD MUSTANG (2025) recall — Visibility
Ford recalls certain Mustangs due to windshield wipers failing in cold weather, reducing visibility and increasing crash risk. Check your VIN for details.
FordJun 30, 2026 - Use cautionVehicle
JEEP GRAND CHEROKEE (2022) recall — Power Train
Chrysler recalls 2022-2024 Jeep Grand Cherokee models with a software error causing gear indicator failure, risking unintended vehicle movement. Owners must update shifter software by August 2026.
ChryslerJun 30, 2026 - Use cautionMedical device
Boston Scientific Corporation recalls Rapid Refill Continuous Injection System, UPN M00566001
Boston Scientific recalls Rapid Refill Continuous Injection System (UPN M00566001) due to risk of syringe loosening or disconnecting from the manifold, potentially causing fluid leakage or procedure delays.
Boston ScientificJun 30, 2026 - Lower riskMedical device
American Contract Systems Inc recalls American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN
American Contract Systems recalls Convenience Kit CV B PACK (Model TNCB10AN) due to catheters not meeting performance specs. Affected units sold until Jan 2027.
American Contract SystemsJun 29, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging systems and equipment. They provide a wide range of products including MRI, CT, X-ray, and ultrasound systems. Their products are used in hospitals and clinics worldwide for diagnostic imaging and patient care.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Jun 29, 2026
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