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- Use cautionMedical device
Contego Medical, Inc recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP
Recalled Neuroguard IEP 3-in-1 carotid stent systems with integrated filter may fail to open during procedures, risking loss of embolic protection. Affected units have specific reference numbers.
Contego MedicalJun 29, 2026 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
GE Healthcare recalls MAC VU360 electrocardiograph models with serial numbers listed. Software issue may cause previous patient data to remain on screen and be incorrectly linked to new patients during use.
GE HealthcareJun 29, 2026 - Use cautionVehicle
TIFFIN OPEN TRAIL (2026) recall — Equipment
Tiffin is recalling 2026 Open Trail RVs with overheating circuit boards that could cause fire. Owners must have the circuit board replaced free by dealers by August 28, 2026.
TiffinJun 29, 2026 - Lower riskVehicle
ENTEGRA VISION (2024) recall — Equipment
Jayco is recalling 2024 Entegra Vision RVs with incorrect weight labels that could lead to overloading and crash risks. Owners will receive free corrected labels by mail.
JaycoJun 29, 2026 - Lower riskDrug
Cipla USA, Inc. recalls Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga,
Cipla USA recalls 30mg Cinacalcet tablets with N-nitroso-cinacalcet above safe daily intake levels. Consumers should contact Cipla for details on affected lots and return instructions.
CiplaJun 29, 2026 - Use cautionVehicle
NISSAN SENTRA (2025) recall — Power Train
Nissan recalls 2025 Sentra vehicles with potential drive power loss and rollaway risk. Owners must have driveshaft inspected and replaced if needed by dealers.
NissanJun 27, 2026 - Stop using nowVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX2 (2026) recall — Latches/Locks/Linkages
DTNA recalls certain 2026-2027 Thomas Built SAF-T-LINER HDX2 buses due to entrance door latch failures. Free dealer repair available.
Thomas Built BusesJun 26, 2026 - Stop using nowVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX2 (2026) recall — Electrical System
DTNA recalls certain 2026-2027 Thomas Built school buses because the entrance door may fail to open or close, increasing injury risk in a crash.
Thomas Built BusesJun 26, 2026 - Use cautionVehicle
ALTEC DIGGER DERRICK (2025) recall — Equipment
Altec is recalling certain 2023-2025 Digger Derrick vehicles due to incorrect pole rack capacity ratings that could increase crash risk during braking or cornering. Owners will receive a safety alert placard by August 21, 2026.
AltecJun 26, 2026 - Lower riskMedical device
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Philips Healthcare recalls specific Incisive CT models with software V4.5 and V5.0 due to potential failure to trigger clinical scans during bolus tracking. Affected units have product codes 728143 or 728144.
Philips HealthcareJun 26, 2026 - Use cautionMedical device
Erbe USA Inc recalls ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Erbe recalls ERBECRYO 2 Cryosurgical Units with serial numbers up to 11608268. A strong pull on the transfer hose may cause CO2 leakage and cryoprobe rupture.
ErbeJun 26, 2026 - Use cautionMedical device
Galt Medical Corporation recalls Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator ,
Boston Scientific recalls transcarotid access kits with potential depth markings that may detach from sheath, causing injury during medical procedures.
Boston ScientificJun 26, 2026 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Syva Emit Disopyramide Assay Enzyme Immunoassay, Lidocaine SMN 10445370 Catalog No 6N319UL
Siemens Healthcare recalls Syva Emit Disopyramide Assay kits with potential low sodium azide risk. Lab technicians may experience mild skin or eye irritation but serious injury is unlikely.
Siemens HealthcareJun 26, 2026 - Lower riskMedical device
Beckman Coulter Inc. recalls REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: -
Beckman Coulter recalls MicroScan LabPro V5.03 Panel Update 11 (US) electronic updates that may cause false antimicrobial susceptibility test results. Affected instruments include MicroScan autoSCAN-4, WalkAway-40 plus, WalkAway-96 plus, and DxM-1040/DxM-1096 models.
Beckman CoulterJun 26, 2026 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog No. 7C219UL
Siemens Healthcare recalls Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls with low sodium azide risk. Lab technicians may experience mild skin or eye irritation from small volumes.
Siemens HealthcareJun 26, 2026 - UnratedDrug
Bionpharma Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc.,
Bionpharma recalls 500mg Divalproex Sodium Delayed-Release Tablets due to foreign tablets present. Affected lots may cause injury if taken.
BionpharmaJun 26, 2026 - Stop using nowFood

Total Nutrition Inc recalls 1. TNVitamins 100% Organic Moringa Capsules 1,200 mg 2. TNVitamins 100% Organic Moringa Powder 96 grams
Total Nutrition Inc recalls two products for Salmonella contamination. Consumers should stop using these items immediately to avoid foodborne illness risks.
Total NutritionJun 26, 2026 - Lower riskDrug
Lannett Company Inc. recalls Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Lannett Company recalls 5mg extended-release dextroamphetamine capsules due to labeling error. Capsules contain only immediate-release pellets but are labeled as extended-release. No immediate action needed but check labels carefully.
Lann: A short, human brand name for headings (e.g.Jun 26, 2026 - Lower riskMedical device
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex
Micro Therapeutics recalls 2 units of Pipeline Flex Embolization Device with Shield Technology (UDI-DI: 00763000448806) due to incorrect diameter labeling. Product is labeled 2.50mm but should be 3.00mm.
Micro TherapeuticsJun 25, 2026 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Ready-To-Eat Chicken Caesar Wrap Products That May Be Contaminated With Listeria
FSIS public health alert: Ready-to-eat chicken Caesar wraps from FRESH SEASONS may be contaminated with Listeria monocytogenes. Products no longer available for purchase; consumers urged not to consume.
FRESH SEASONSJun 25, 2026 - Use cautionMeat & poultry
Reser’s Fine Foods, Inc. Recalls Ready-To-Eat Pasta Salad Product Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 5,300 pounds of Reser's pasta salad products that may contain undeclared chicken, egg, and milk allergens. Consumers urged to stop using these products immediately.
Reser'sJun 25, 2026 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Boneless Chicken Breast Product Due to Misbranding and Undeclared Allergens
FSIS public health alert: Boneless chicken breast products contain undeclared eggs, a known allergen. Consumers urged not to consume these products; discard or return to retailer.
FW Farms LLCJun 25, 2026 - Stop using nowPet food

Breeder’s Edge, Shelter’s Choice – Canine milk replacer: Variable levels of Vitamin D
Revival Animal Health recalls Breeder's Edge and Shelter's Choice canine milk replacers due to variable Vitamin D levels that may cause rickets or kidney issues in dogs. Stop feeding affected products immediately.
Revival Animal HealthJun 25, 2026 - Stop using nowMedical device
C.R. Bard Inc recalls Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314
Bard recalls certain Foley catheter trays and related products that contain Pericare wipes with contamination. Affected units include specific model numbers and UDI codes. Consumers should stop using these products to avoid potential health risks.
BardJun 25, 2026 - Lower riskFood
Publix Super Markets, Inc. recalls Organic Whole Blueberries, Net Wt. 48 oz (3Lb) plastic bag, packed in 6 bags per case of 10 oz each. Keep Frozen. UPC
Publix recalls organic blueberries with potential E. coli O145:H28 contamination. Products with expiration date before Feb 9, 2028 are affected. Consumers should check UPC 41415-12053.
PublixJun 25, 2026 - Use cautionMedical device
Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK Software Version: 2.0.11, new version:
Quantum Rehab recalls R-TRAK wheelchair software version 2.0.11 due to potential unexpected stops when driving, which could cause falls or injuries. Affected units may need software update to 2.0.13.
Quantum RehabJun 25, 2026 - Use cautionMedical device
ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory
ResMed recalls Astral 100/150 and 100/50 ventilators due to supercapacitor electrolyte leakage that may damage charger chips, causing ventilation interruptions. Affected units have specific serial numbers and model codes.
ResMedJun 25, 2026 - Lower riskFood

GELLERT GLOBAL GROUP recalls Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea:
Gellert Global Group recalls 12-packs of Kimbap products due to undeclared fish allergen. Consumers should check packaging for the recall and avoid products with fish.
Gellert Global GroupJun 25, 2026 - Lower riskDrug
Bell Pharmaceuticals, Inc recalls QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included (NDC 63868-026-15); b) 1
Bell Pharmaceuticals recalls QC Quality Choice carbamide peroxide 6.5% (0.5 fl oz) due to subpotent drug content. Products may have low pH and reduced effectiveness, risking inadequate treatment. Consumers should check NDC numbers and lot dates for affected items.
Bell PharmaceuticalsJun 25, 2026 - Lower riskFood
Fresh & Ready Foods LLC recalls Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1 00000 01015 0. Manufactured
Fresh & Ready Foods recalls Burger Chicken Fillet (SKU 10150) after raw chicken patties were used, posing Salmonella risk. Consumers should check UPC 1 00000 01015 0 and lot 26171.
Fresh & Ready FoodsJun 25, 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.