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
POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC recalls SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Polymedco recalls SEDIPLAST diagnostic tubes S-100 and S-1000 due to potential blood release if tube cap detaches during use. Affected units were distributed worldwide, including US states and UK.
PolymedcoAug 25, 2026 - Stop using nowVehicle
FORD BRONCO SPORT (2026) recall — Structure
Ford recalls certain 2026 Bronco Sports due to improperly tightened vehicle joints. This defect can cause loss of control, electrical failure, or detached parts.
FordAug 25, 2026 - Use cautionVehicle
FORD BRONCO (2026) recall — Engine And Engine Cooling
Ford is recalling 2026 Bronco vehicles with engine piston dome issues that may cause power loss and crash risk. Owners must have their engine inspected and repaired by dealers.
FordAug 25, 2026 - Lower riskFood
Quality Dairy Farms Inc. recalls Mercer's brand 6 ICE CREAM SANDWICHES TO GO; packaged in clear plastic; ice cream sandwiches may be rolled in peanuts
Quality Dairy Farms Inc. recalls Mercer's 6-piece ice cream sandwiches due to undeclared peanuts visible through clear packaging. Consumers should check for peanuts in the product.
Mercer'sAug 25, 2026 - Stop using nowFood
Optimus Inc. d/b/a/ Markys Caviar recalls Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2
Markys Caviar recalls 2 units of Mon Sire Brie cheese due to Listeria monocytogenes contamination. Keep refrigerated until expiration dates.
Markys CaviarAug 25, 2026 - Lower riskDrug
Ajanta Pharma USA Inc recalls Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc.,
Ajanta Pharma recalls 100-count Fluphenazine Hydrochloride tablets due to impurity levels exceeding safety limits. Affected lots have specific expiration dates and are prescription-only.
Ajanta PharmaAug 25, 2026 - Use cautionVehicle
FORD MUSTANG (2025) recall — Electrical System
Ford is recalling certain 2024-2026 Mustang vehicles due to potential loss of driver power and lighting/windshield washing system function, increasing crash risk. Owners must contact Ford for free wiring harness repairs.
FordAug 25, 2026 - Lower riskMedical device
Neuronetics, Inc. recalls NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below
Neuronetics recalls NeuroStar Advanced Therapy Systems with HP Coil Assembly Part Number 81-01000-200 due to cables not meeting product specifications. Affected units include specific models and software versions.
NeuroneticsAug 24, 2026 - UnratedMedical device
Limitless Cryo Spa LLC recalls Glypto Device, Glypto Cryo Machine;
Limitless Cryo Spa LLC recalls 219 Glypto Cryo Machines due to lack of 510(k) clearance. This device may not be safe for medical use without proper regulatory approval.
Limitless Cryo SpaAug 24, 2026 - UnratedMedical device
Olympus Corporation of the Americas recalls Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A.
Olympus recalls 72 units of M3 Gold Autoclavable Foroblique Telescope 30 (Model M3-30A) due to sterilization parameter discrepancies between instructions and Japanese package inserts.
OlympusAug 24, 2026 - Use cautionMedical device
ASP Global, LLC. recalls Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:
ASP Global recalls Expressaire tourniquet cuffs due to incorrect expiration dates. Products labeled with a 10-year shelf life actually have a 5-year validated life.
ExpressaireAug 24, 2026 - Stop using nowVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX2 (2027) recall — Structure
DTNA recalls 2027 Thomas Built SAF-T-LINER HDX2 and EFX2 school buses due to missing connector plates that may compromise seat belt anchors and body joint strength.
Thomas Built BusesAug 24, 2026 - Stop using nowMedical device
Boston Scientific Corporation recalls Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5;
Boston Scientific recalls specific Imager II Angiographic Catheters models due to risk of tip fracture leading to device fragments remaining in patients or migrating through vasculature, potentially causing life-threatening embolism.
Boston ScientificAug 24, 2026 - Lower riskDrug
ImprimisRx NJ LLC recalls Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only,
ImprimisRx recalls 10mL ophthalmic solution with subpotent drug risk. This may not work as intended for eye procedures. Check NDC 71384-732-10 and lot numbers for affected products.
ImprimisRxAug 24, 2026 - UnratedDrug
Teva Pharmaceuticals USA, Inc recalls traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o,
Teva Pharmaceuticals recalls 50mg traZODone tablets manufactured in Croatia due to foreign tablets present. Consumers should contact Teva for details.
TevaAug 24, 2026 - UnratedDrug
Hikma Pharmaceuticals USA INC. recalls Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05)
Hikma Pharmaceuticals recalls 10mg Ramipril capsules due to failed impurities test. Products may contain dicyclohexylurea (DCU) which could cause harm. Check NDC codes 76282-673-01 or 76282-673-05 for affected lots.
Hikma PharmaceuticalsAug 24, 2026 - Lower riskFood
International Sprout Holdings, Inc recalls Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506
US alfalfa bags from International Sprout Holdings may contain E. coli and Salmonella. Consumers should check lot numbers and contact the company for recalls.
International Sprout HoldingsAug 23, 2026 - Lower riskFood
Everything Sprouts, LLC recalls Everything Sprouts Crunchy Protein Sprout Mix, containing Alfalfa Fenugreek, Cabbage, Mung, Adzuki, Lentils, Green Pea,
Everything Sprouts recalls crunchy protein sprout mix due to potential STEC E. coli and Salmonella contamination. Consumers should avoid using affected lots.
Everything SproutsAug 22, 2026 - Stop using nowVehicle
KENWORTH T680 (2027) recall — Seats
PACCAR recalls certain 2027 Kenworth T680 vehicles due to seat ventilation harness fire risk. Dealers will replace the harnesses free of charge.
KenworthAug 22, 2026 - Use cautionVehicle
KIA EV9 (2025) recall — Air Bags
Kia is recalling 2025-2026 EV9 vehicles with a front air bag that may not deactivate during crashes with children in the front seat, risking injury. Owners must have air bag system inspected and repaired by dealers.
KiaAug 22, 2026 - UnratedMedical device
SI-BONE, Inc. recalls iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm),
SI-BONE recalls 100 units of iFuse TORQ Implant System with specific model numbers and lots due to potential sterility issues from packaging seal failures.
SI-BONEAug 21, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model
Philips recalls Spectral CT 7500 RT systems with specific software versions and model numbers due to potential image artifacts and incorrect slice thickness. Affected units may require software updates to prevent safety issues.
PhilipsAug 21, 2026 - Stop using nowVehicle
ALTEC DIGGER DERRICK (2025) recall — Forward Collision Avoidance
Altec recalls certain Digger Derrick vehicles due to improperly calibrated automatic braking systems that may delay response, increasing crash risk.
AltecAug 21, 2026 - Lower riskMedical device
Philips North America Llc recalls Achieva 3.0T; Model Numbers (REF): 1. 781177, 2. 781277, 3. 781278, 4. 781344, 5. 781345;
Philips recalls Achieva 3.0T MRI scanners with specific model numbers due to a software issue that can terminate scans during image reconstruction if scan parameters are manually adjusted.
PhilipsAug 21, 2026 - Lower riskMedical device
Midmark Corporation recalls Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,
Midmark recalls IQvitals Zone blood pressure monitors with model numbers 1-200-03300 and 1-200-0330 that may give inaccurate blood pressure readings when using the Linear Deflation Method. Affected units were sold between 2020 and 2023.
MidmarkAug 21, 2026 - Stop using nowPet food
Fromm – Fromm wet canned dog food: Potential metal contamination
Fromm Family Foods is recalling 3,852 cases of Turkey Pâté and 1,973 cases of Milo's Meatloaf Pâté wet dog food due to potential metal contamination. Dogs may experience choking, vomiting, or internal injuries if metal is ingested.
FrommAug 21, 2026 - Stop using nowDrug
VITRUVIAS THERAPEUTICS INC recalls Thyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyronine (T3) 4.5 mcg,
Vitruvias Therapeutics recalls thyroid tablets with superpotent drug levels. These tablets may cause serious health issues if taken without medical supervision.
Vitruvias TherapeuticsAug 21, 2026 - Use cautionDrug
Golden State Medical Supply Inc. recalls Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA,
Golden State Medical Supply recalls Prasugrel HCl 10mg tablets due to failed dissolution specifications. Check lot GS062298.
Golden State Medical SupplyAug 21, 2026 - UnratedDrug
Lexia LLC recalls Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4
Broadway Joe's recalls 3000g CBD pain cream due to potential raw material contamination. Affected lots expire January 2027. Consumers should check product labels for lot numbers.
Broadway Joe'sAug 21, 2026 - Use cautionVehicle
FORD F-650 SD (2025) recall — Structure
Ford F-650 SD 2025 vehicles with liftgate platform falling risk. Recall due to deck pins breaking, causing potential injury. Free fix by Marathon Industries.
FordAug 21, 2026
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
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.