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- Lower riskMedical device
AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number:
AVID Medical recalls Halyard IV Start Kits with possible open seals on BD ChloraPrep applicators. Affected kits may have packaging that doesn't seal properly, risking contamination. Stop using immediately if you own these kits.
AVID MedicalJul 22, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number:
AVID Medical recalls 48-unit Halyard IV Start Kits (model KRIV26-02) due to possible Aspergillus penicillioides contamination. Affected kits may cause infections if used improperly.
AVID MedicalJul 22, 2026 - Use cautionMedical device
Boston Scientific Corporation recalls Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)
Boston Scientific recalls StoneSmart Connect Console power adapters with higher-than-expected grounding resistance that may fail electrical safety tests during installation. Affected units include specific model numbers and serial ranges.
Boston ScientificJul 22, 2026 - Lower riskMedical device
FUJIFILM Healthcare Americas Corporation recalls FUJIFILM Synapse PACS software v7.4.310; radiological image processing system
FUJIFILM recalls software version v7.4.310 for inaccurate ruler measurements in radiological image processing systems. Affected units include specific serial numbers and UDI codes.
FUJIFILMJul 22, 2026 - Lower riskMedical device
Merge Healthcare, Inc. recalls Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
Merge Healthcare recalls medical imaging workstations with software version V9.5 for inaccurate measurements. Affected units may display incorrect diagnostic data.
Merge HealthcareJul 22, 2026 - Lower riskFood
Coast Citrus Distributors recalls Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes
Coast Citrus Distributors recalls bulk jalapeno peppers from July 1-31, 2026 due to potential Salmonella Javiana contamination. Consumers should check UPCs and pack dates for affected products.
Coast Citrus DistributorsJul 22, 2026 - Lower riskFood
Lidl US TRADING recalls ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling. Product is packed onto a
Lidl US recalls Greek Style Shortbread Cookies with undeclared wheat, soy, milk, eggs and tree nuts (coconut) sold in US stores. Consumers should check labels for foreign language text and avoid if allergic.
LidlJul 22, 2026 - Use cautionFood
MIDWEST POULTRY SERVC C/O H & LELECTRIC recalls Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Truth, Natural Cage Free Grain
Recalled Simple Truth Natural Cage Free Brown Eggs may contain Salmonella Enteritidis. Check UPCs and dates to avoid illness. Stop using if affected.
Midwest Poultry ServiceJul 22, 2026 - Lower riskDrug
MICRO LABS USA INC recalls Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro
Micro Labs USA recalls 2% Dorzolamide and 0.5% Timolol eye drops due to broken cap spikes causing undeliverable drops. Rx-only medication with specific lot number and expiration date.
Micro LabsJul 22, 2026 - Use cautionVehicle
VOLKSWAGEN ATLAS (2025) recall — Back Over Prevention
Volkswagen recalls 2024-2026 Atlas vehicles for rearview camera software issues that may cause image failure, increasing crash risk. Owners receive free updates.
VolkswagenJul 22, 2026 - Use cautionVehicle
FORD EXPLORER (2025) recall — Seats
Ford is recalling 2025-2027 Explorer and Aviator vehicles with driver seats that may unintentionally recline, potentially trapping second-row occupants. Owners must contact Ford for free repairs to disable the seat module.
FordJul 21, 2026 - Use cautionVehicle
FORD BRONCO (2021) recall — Engine
Ford recalls 2021-2026 Bronco and Bronco Raptor vehicles due to engine wiring short circuits that could cause fire. Owners must contact Ford for free repairs by specific dates.
FordJul 21, 2026 - Use cautionVehicle
BLUE BIRD VISION TRANSIT BUS (2025) recall — Service Brakes, Hydraulic
Blue Bird is recalling certain 2022-2027 Vision transit buses due to a brake fluid leak hazard that could cause fire or crash risk. Owners must contact Blue Bird for free repairs.
Blue BirdJul 20, 2026 - Use cautionMedical device
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;
Mirion recalls Captus 4000e Thyroid Uptake Systems (models 5430-30151, 5430-30152, 5430-30154) due to potential tension bolt failure causing spring arm to drop 25 inches. Affected units shipped April 2019–Feb 2024 with serial numbers 940548–941398.
MirionJul 20, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KIT 2 W/CONNECT DYNDH1487A
Medline recalls convenience kits containing BD ChloraPrep Clear 1mL applicators from specific lots due to potential open seals causing infections. Affected kits may lead to skin or systemic infections if used.
MedlineJul 20, 2026 - Stop using nowMedical device
SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068
Dentsply Sirona Capsule Mixer Model 5546068 may cause electrical discharge when unplugged. Affected units have UDI:9336472005542 or serial numbers 0003-1533. Stop using immediately to avoid electrical hazards.
SDI LimitedJul 20, 2026 - Lower riskMedical device
Midmark Corporation recalls Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions
Midmark recalls specific IQecg ECG models with outdated software that may show incorrect heart rate readings. Affected units include certain serial numbers and software versions. Update to v10.1.0.18 or later to fix.
MidmarkJul 20, 2026 - Use cautionMedical device
GE Medical Systems Information Technologies Inc recalls PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353
GE Medical Systems recalls Portrait Core Services Software V1.0.5 (Ref# 5697353) due to potential loss of patient monitoring and alarm reset issues. Affected units may require software updates to prevent safety risks.
GE Medical SystemsJul 20, 2026 - Lower riskMedical device
Paragonix Technologies Inc. recalls Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001
Paragonix recalls its KidneyVault Portable Renal Perfusion System (REF# PRGNX-8008-001) due to a firmware defect that may cause a blank screen and loss of preservation parameters. Affected units have specific serial numbers and software versions.
ParagonixJul 20, 2026 - Lower riskFood
Piazza Produce (dba CIBUS Fresh) recalls Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253
Cibus Fresh recalls Garden Salad products with possible Cyclospora contamination. Consumers should check UPC 810028250253 and discard if purchased before July 2026.
Cibus FreshJul 20, 2026 - Use cautionVehicle
BLUE BIRD VISION SCHOOL BUS (2026) recall — Service Brakes, Hydraulic
Blue Bird recalls 2022-2027 Vision school buses with potential brake fluid leaks that could cause fires or crashes if hot engine components contact brake lines.
Blue BirdJul 20, 2026 - Lower riskFood
FACTORY6, INC. recalls Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle.
Zen Principle recalls 180-capsule Moringa Leaf Powder due to possible Salmonella contamination. Consumers should check product codes and follow safety steps.
Zen PrincipleJul 19, 2026 - Lower riskFood
M.G. Foods, Inc. recalls Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2
M.G. Foods recalls Spicy Breakfast Burritos containing undeclared soy in sausage. Consumers should check labels for soy ingredients and avoid products with unlisted soy.
FRESH & READY FOODSJul 18, 2026 - Stop using nowMedical device
SPECTRUM MEDICAL SRL recalls Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W Model/Catalog
Spectrum Medical recalls Quantum PureFlow Standard Heat Exchangers due to a blood-to-glycol leak hazard. Check lot code 18051160302205.
Spectrum MedicalJul 17, 2026 - Stop using nowVehicle
ALTEC AT SERIES (2025) recall — Equipment
Altec recalls 2024-2026 AT Series vehicles due to improperly heat-treated fasteners that may fail, causing separation of the pedestal and turntable.
AltecJul 17, 2026 - Use cautionVehicle
IC BUS CECB (2025) recall — Structure
International recalls certain 2025-2027 IC Bus CECB transit buses due to potential body panel separation in crashes, risking injury. Dealers will install free rivets to fix the joint strength issue.
InternationalJul 17, 2026 - Stop using nowFood
Botticelli Foods, LLC recalls bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961
Botticelli Foods recalls bettergoods Pistachio Nut Butter (6.7oz) due to potential Salmonella contamination. Check your UPC and lot code.
bettergoodsJul 17, 2026 - Lower riskFood
Taylor Farms de Mexico S. de R.L. de C.V. recalls SYSCO LETTUCE CHOP 4/5# SYSCO LETTUCE SHRED 1/8" 4/5# Iceberg only products.
Taylor Farms recalls certain lettuce products due to potential Cyclospora contamination. Consumers should check product dates and stop using affected items to avoid foodborne illness.
Taylor FarmsJul 17, 2026 - Lower riskMedical device
Remel Europe Ltd. recalls Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics
Thermo Fisher Diagnostics recalls Neisseria meningitidis Gp C 2ml/VL test kits with Product Number R30166901 that may not detect bacteria within 60 seconds. Affected lots have specific expiration dates.
RemelJul 17, 2026 - Stop using nowDrug
Sunny Pharmtech Inc. recalls Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove
Sunny Pharmtech recalls Cyclophosphamide injection vials due to stainless steel particles that could cause serious injury. Affected vials were manufactured in Taiwan with specific lot numbers.
Sunny PharmtechJul 17, 2026
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83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.