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
35,025 found- Use cautionVehicle
VOLKSWAGEN TIGUAN (2024) recall — Back Over Prevention
Volkswagen recalls 2024 Tiguan vehicles with rearview camera software error that may not display images, increasing crash risk. Owners must update software free of charge.
VolkswagenMay 20, 2026 - Use cautionVehicle
TOYOTA TUNDRA (2024) recall — Engine And Engine Cooling
Toyota recalls 2024 Tundra vehicles with V35A engines due to potential engine failure causing loss of drive power and crash risk. Owners must have inspection and possible repair by dealers.
ToyotaMay 20, 2026 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS icono floor. Model Number: 11327700.
Siemens recalls ARTIS icono floor model 11327700 due to potential loss of movement capability after adjusting detector lift height to max or min limits. Affected units have specific serial numbers.
SiemensMay 20, 2026 - Use cautionMedical device
Insulet Corporation recalls Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2. POD-OMNI-I1-6220. 3. OMNI-I1-6729
Insulet recalls Omnipod 5 Pods with specific model numbers due to manufacturing defect causing insulin leaks, potentially leading to high blood sugar and serious health risks.
InsuletMay 20, 2026 - Lower riskMedical device
Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241
Zimmer recalls Off-Axis Comprehensive Shoulder System model 110040241 due to plastic guides catching during reaming, causing breakage. Five complaints reported.
ZimmerMay 20, 2026 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayCare 2024A SP1. Oncology Information Systems.
RaySearch Laboratories recalls RayCare 2024A SP1 software version 8.0.1.60193 due to potential data loss if beam set delivery notes are modified during treatment sessions.
RaySearch LaboratoriesMay 20, 2026 - Lower riskFood
Hometown Food Company recalls Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case
Hometown Food Company recalls Birch Benders Sweet Potato Pancake and Waffle Mix due to undeclared egg. Check your 12oz bags with UPC 8 1000156076 8 for affected lots.
Hometown Food CompanyMay 20, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls 1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5)
AVID Medical recalls Ritmed Neurological Sponges (models 55992C-55998C) due to potential for unexpected endotoxin levels. Consumers should check product labels for model numbers and lot numbers.
AVID MedicalMay 19, 2026 - Lower riskMedical device
American Contract Systems Inc recalls American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK - 208400, Model Item Number
Recall of specific medical procedure kits due to potential for unexpected endotoxin levels in Ritmed Neurological Sponges. Affected items include CRANI PACK, SPINE PACK, and other surgical trays with listed model numbers and lot numbers.
American Contract SystemsMay 19, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
AVID Medical recalls Halyard STANDARD LINE INSERTION PACK model PVHM234-01 due to silicone seal defects that may cause fluid leakage or occlusion. Affected units include specific lot numbers with expiration dates.
AVID MedicalMay 19, 2026 - Use cautionVehicle
TESLA MODEL Y (2025) recall — Equipment
Tesla is recalling certain 2025-2026 Model Y vehicles due to missing certification labels that could lead to unintentional vehicle overloading and crash risk. Owners received notification letters mailed July 17, 2026.
TeslaMay 19, 2026 - Use cautionVehicle
HYUNDAI IONIQ 5 (2025) recall — Suspension
Hyundai is recalling certain 2025 Ioniq 5 vehicles due to rear suspension fasteners that may loosen and detach, increasing crash risk. Owners will receive free inspections and alignments by July 17, 2026.
HyundaiMay 19, 2026 - Use cautionVehicle
HYUNDAI SANTA CRUZ (2025) recall — Forward Collision Avoidance
Hyundai recalls certain 2025-2026 Santa Cruz vehicles for potential premature braking in forward collision avoidance systems. Owners will receive free software updates by July 17, 2026.
HyundaiMay 19, 2026 - Lower riskMedical device
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes.
Depuy recalls ATTUNE Revision Hinge Knee Insert Components with specific part numbers and lot numbers due to potential sterility compromise in packaging.
DepuyMay 19, 2026 - Use cautionMedical device
W L Gore & Associates, Inc. recalls GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes
W L Gore recalls specific Thoracic Branch Endoprosthesis Side Branch Components (TSB081006A, TSB081206A, etc.) due to catheter separation risk. Affected units include certain model numbers sold in US, Canada, EMEA, Australia, New Zealand, Japan, China, and Taiwan.
W L GoreMay 19, 2026 - Lower riskMedical device
Howmedica Osteonics Corp. recalls TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
Howmedica recalls Triathlon Universal Baseplate Size 3 (part 5521-B-300) due to labeling errors causing confusion with Size 4 models. Affected units may have incorrect lot numbers.
HowmedicaMay 19, 2026 - Lower riskMedical device
Medtronic Navigation, Inc.-Boxborough recalls Medtronic O-arm O2 Imaging System. Model Number: BI70002000.
Medtronic recalls O-arm O2 Imaging System model BI70002000 due to potential image artifacts from a detector panel firmware anomaly. Affected units have specific serial numbers listed in the recall notice.
MedtronicMay 19, 2026 - UnratedDrug
Shimoga Chemicals recalls Clomiphene Citrate USP Active Pharmaceutical Ingredient (CAS : 50-41-9), Net Weight a)1 KG (NDC 84849-000-01), b) 500 g
Shimoga Chemicals recalls Clomiphene Citrate USP Active Pharmaceutical Ingredient due to cGMP deviations. This is a drug product for medical use only.
Shimoga ChemicalsMay 19, 2026 - Lower riskFood
Kettle Cuisine, LLC recalls Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ
Whole Foods Market Kitchens Minestrone Soup (24 oz) contains undeclared shrimp. Recalled due to allergen risk. Check product labels for lot numbers.
Kettle CuisineMay 19, 2026 - Stop using nowFood
Rich Products Corp recalls Farm Rich Pizza Cheese Crunchers
Rich Products Corp recalls Farm Rich Pizza Cheese Crunchers due to potential metal contamination. Check your lot numbers and UPC codes immediately.
Farm RichMay 19, 2026 - Lower riskFood
Refresqueria Estrella Inc. recalls ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL.
Refresqueria Estrella recalls multiple sizes of Passion Fruit Drink due to undeclared FD&C Red 40. Consumers should check production dates and lot codes for affected products.
EstrellaMay 19, 2026 - Lower riskMedical device
Bioporto Diagnostics A/S recalls ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.
Bioporto recalls ProNephro AKI Reagent Kit (100 tests) due to potential missed kidney disease diagnoses from improper reagent use. Affected units include specific model numbers and lot numbers.
BioportoMay 18, 2026 - Use cautionVehicle
KEYSTONE MONTANA (2026) recall — Suspension
Keystone recalls 2024-2026 Montana RVs with potentially loose shock bolts that could cause loss of stability and crash risk. Owners must contact dealers for free bolt replacement.
KeystoneMay 18, 2026 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034
Philips recalls specific MultiDiagnost Eleva models due to hand switch button not fully releasing, which may cause loss of imaging or unintended radiation exposure. Affected models include 708032-708038.
PhilipsMay 18, 2026 - Lower riskMedical device
DeRoyal Industries Inc recalls DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
DeRoyal recalls Covaderm Plus vascular dressings due to potential lack of sterility. Affected units may cause infection if used improperly.
DeRoyalMay 18, 2026 - Lower riskMedical device
WALLAC OY recalls GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL),
WALLAC recalls GSP Neonatal GALT Kit (product codes 3303-001U, 3303-0010) due to reduced on-board stability that may cause run-QC failures and delay patient result reporting.
WALLACMay 18, 2026 - Use cautionMedical device
Abiomed, Inc. recalls Impella CP Set with SmartAssist. Product Codes: 1000080, 1000851, 0048-0014, 0048-0024-JP.
Abiomed recalls Impella CP Set with SmartAssist (product codes 1000080, 1000851, 0048-0014, 0048-0024-JP) due to potential persistent low purge pressure alarms and interruption of mechanical circulatory support.
AbiomedMay 18, 2026 - UnratedDrug
PReye LLC recalls PReye Vitamin See Antioxidant Preservative Free Eye Drops, Distributed by: PReye, LLC, Golden, CO
PReye Vitamin See Antioxidant Preservative Free Eye Drops recalled due to lack of sterility assurance. All lots within expiry date are affected.
PReyeMay 18, 2026 - UnratedDrug
AbbVie Inc. recalls PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie
AbbVie recalls 2,736 bottles of PRED MILD prednisolone acetate ophthalmic suspension due to failed stability specifications. Check your lot numbers.
AbbVieMay 18, 2026 - Lower riskDrug
IntegraDose Compounding Services LLC recalls Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC. 3650 Victoria St N,
IntegraDose recalls Vasopressin 2 Units/2mL in 0.9% Sodium Chloride due to subpotent drug risk. Affected lots have specific NDC and expiration dates. Contact for remedy.
IntegraDoseMay 18, 2026
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