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
34,956 found- Stop using nowMedical device
COVIDIEN LLC recalls 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve), Model Number 36826
Covidien recalls 8Fr Safe Grad Cat W/Valve (Argyle Suction Catheter Kits with Chimney Valve) Model 36826 due to import refusal. Affected units sold with Lot 1816211: stop using immediately.
CovidienNov 5, 2018 - Use cautionMedical device
Capintec Inc recalls Captus 700 Thyroid Uptake System, Model # 5430-3137 and 5430-3138
Capintec recalls specific models of thyroid uptake systems due to potential spring arm failure from broken tension rods, risking the collimator falling 25 inches.
CapintecNov 5, 2018 - Lower riskDrug
Kadesh International recalls puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
Kadesh International recalls EYE RELIEF DROPS due to non-sterile manufacturing. All bottles without expiration dates are affected. Consumers should contact the company for details.
KadeshNov 5, 2018 - Stop using nowFood
Bakkavor Foods USA Inc. recalls Baked Macaroni and Cheese, NET WT 12 OZ (340g), CONTAINS: WHEAT, MILK, EGG, Produced By BAKKAVOR USA, 2700 Westinghouse
Bakkavor recalls 12 oz Baked Macaroni and Cheese due to undeclared lobster, shrimp, and soy. Check your label for allergen info.
BakkavorNov 5, 2018 - Lower riskFood
Cedar Lake Tea recalls Apricot Chai Tea, 8 oz. Loose. UPC 41427-96317
Cedar Lake Tea recalls Apricot Chai Tea (8 oz. loose) with UPC 41427-96317 due to potential glass contamination. Consumers should check product details and contact the company for guidance.
Cedar Lake TeaNov 5, 2018 - Lower riskFood
ConAgra Foods, INc. recalls Duncan Hines Classic Classic Yellow cake mix 15.25oz. 12 retail units per case 644209307494
ConAgra Foods recalls Duncan Hines Classic Yellow cake mix due to Salmonella found in retail samples. Consumers should check product codes and follow safety steps.
Duncan HinesNov 5, 2018 - Use cautionVehicle
AUDI Q5 (2017) recall — Engine And Engine Cooling
Audi is recalling 2017 Q5 vehicles with a risk of fire from a blocked or short-circuited coolant pump. Owners must contact Audi for free pump replacement.
AudiNov 4, 2018 - Stop using nowMedical device
Virtual Imaging, Inc. recalls RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product Usage: Instrument is used to take diagnostic
Virtual Imaging recalls RadPRO Mobile 40kW Digital X-Ray System Model SM-40HF-B-D-C due to risk of tube head falling off during use. Affected units may need immediate action to prevent injury.
Virtual ImagingNov 2, 2018 - Lower riskMedical device
Baxter Healthcare Corporation recalls GEM Coupler Forceps, GEM4183C, packaged individually.
Baxter Healthcare recalls GEM4183C Coupler Force: Potential rust on forceps may cause issues. Check product code and lot numbers for affected items.
Baxter HealthcareNov 2, 2018 - Use cautionMedical device
Stephanix recalls STEPHANIX D2RS Digital Dynamic Remote Systemhttp://cts.fda.gov/division-tracking/images/trash.png Product The D2RS
Stephanix recalls D2RS Digital Dynamic Remote System due to potential continued movement after command release, risking unintended motion during medical procedures.
StephanixNov 2, 2018 - Lower riskMedical device
Ascom (US) Inc. recalls Ascom Telligence Nurse Call System
Ascom recalls Telligence Nurse Call System version 5.0 (Build 5:0.4) due to potential communication failure with hallway devices, causing unreported device failures.
AscomNov 2, 2018 - UnratedMedical device
CIVCO Medical Instruments Co., Inc. recalls SonoSite FUJIFILM Needle Guide Bracket, REF number P06013-08, Reusable non-sterile bracket for use with SonoSite L25
Civco Medical Instruments recalls SonoSite FUJIFILM Needle Guide Brackets with lot numbers A000012-A050663. These reusable brackets may cause injury if not used properly with SonoSite L25 transducers.
Civco Medical InstrumentsNov 2, 2018 - UnratedDrug
Golden State Medical Supply Inc. recalls IRBESARTAN Tablets, USP 300 mg (a) 30-count bottle (NDC 60429-642-30), (b) 90-count bottle (NDC 60429-642-90) Rx Only,
FDA confirms N-nitrosodiethylamine (NDEA) impurity in Golden State Medical Supply's 300mg IRBESARTAN tablets. Rx-only bottles with specific NDC numbers and lot dates are affected. Consumers should contact the manufacturer for details.
Golden State Medical SupplyNov 2, 2018 - Lower riskDrug
Sandoz Inc recalls Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, packaged in a) 100-capsule bottles (NDC 0185-0122-01);
Sandoz recalls 100mg Nitrofurantoin Capsules due to cross contamination risk. Affected lots expire March 2020. Consumers should contact Sandoz for details.
SandozNov 2, 2018 - Use cautionDrug
Bound Tree Medical, LLC recalls Curaplex Epi Kit NOT FOR IV USE, #8600-01120, Epi-Safe Kit 8600-01 120 contains:2 Safety-LOK Syringe, TB, 1cc w/
Bound Tree Medical recalls Epi-Safe Kit 8600-01120 due to incorrect dosage instructions for children under 33 lbs. that may lead to unsafe epinephrine administration during anaphylaxis. Affected kits contain Safety-LOK Syringes with unapproved dosage markings.
Bound Tree MedicalNov 2, 2018 - Lower riskFood
Red Bull North America Inc. recalls Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine,
Red Bull North America recalls specific batches of 8.4 oz energy drinks due to off taste, color, and excessive ingredient levels.
Red BullNov 2, 2018 - Lower riskFood
Fairview Mills Inc recalls DIDGFPGB, Food Grade Pre-Gel Corn Flour. Bulk
Fairview Mills recalls bulk food-grade pre-gel corn flour due to undetected gluten. The product does not list wheat on its label, posing a risk for gluten-sensitive individuals.
Fairview MillsNov 2, 2018 - Lower riskFood
Frito-Lay, Inc. recalls 16 count Crunch & Pop Mix Variety Pack Sack
Frito-Lay recalls 16-count Crunch & Pop Mix Variety Packs with potential undeclared milk due to cheese-flavored chips. Consumers should check for specific use-by dates and manufacturing codes.
Frito-LayNov 2, 2018 - Use cautionVehicle
MITSUBISHI FUSO FEC52 (2012) recall — Equipment
Mitsubishi Fuso Fuso FEC52 (2012) trucks with defective fire extinguishers may not function properly during fires, increasing injury risk. Owners must contact MFTA for a free replacement.
Mitsubishi FusoNov 1, 2018 - Stop using nowVehicle
FORD MUSTANG (2013) recall — Air Bags
Ford is recalling 2013 Mustang vehicles with passenger air bag inflators that may explode due to humidity and temperature exposure, risking serious injury or death. Owners must stop driving until repaired.
FordNov 1, 2018 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Equipment
Pierce is recalling 2015-2016 Arrow XT emergency vehicles with Hale pressure relief valves due to potential water pressure reduction affecting fire fighting. Owners must contact Pierce or Hale for free remedy kit installation.
PierceNov 1, 2018 - Use cautionVehicle
CHRYSLER PACIFICA (2017) recall — Electrical System
Chrysler recalls 2017 Pacifica vehicles with 3.6L engines due to potential engine stall causing crash risk. Owners will receive free software update.
ChryslerNov 1, 2018 - Use cautionVehicle
JEEP GRAND CHEROKEE (2018) recall — Fuel System, Gasoline
Chrysler recalls 2018 Jeep Grand Cherokee Trackhawk vehicles with a potential fuel line separation risk, causing engine stalls and fire hazards. Owners must have fuel lines inspected or replaced by dealers.
ChryslerNov 1, 2018 - Use cautionVehicle
FOREST RIVER CHEROKEE (2018) recall — Electrical System
Forest River recalls 2017-2018 Cherokee travel trailers with electrical wiring issue that could cause fire if wires are connected to same lug. Owners must have wire relocated by dealer.
Forest RiverNov 1, 2018 - Use cautionMedical device
LivaNova USA Inc. recalls SORIN Heater-Cooler System 3T 120V~/60Hz REF 16-02-85 Description of product: The St¿ckert Heater-Cooler System is an
LivaNova recalls SORIN Heater-Cooler System 3T models with potential disinfectant inefficiency and aerosol emission risks. Affected units may need repair or replacement to ensure patient safety during medical procedures.
LivaNovaNov 1, 2018 - Lower riskMedical device
R & D Systems, Inc. recalls Quantikine¿ IVD¿ ELISA, Human sTfR Immunoassay kit. Product Usage: The QuantikineTM IVDTM sTFR Enzyme linked
R&D Systems recalls Quantikine sTfR ELISA Kit (catalog DTFR1, lot P180851) due to incorrect control data card number. This may affect lab results accuracy for iron deficiency anemia testing.
R&D SystemsNov 1, 2018 - Lower riskMedical device
Boston Scientific Corporation recalls The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The
Boston Scientific recalls SQ-RX Pulse Generator (Model 1010) for accelerated battery depletion due to internal malfunctions, potentially shortening replacement intervals. Affected patients should contact for guidance.
Boston ScientificNov 1, 2018 - Lower riskMedical device
ORTHO-CLINICAL DIAGNOSTICS recalls VITROS NT-proBNP Reagent, Cat No. 6802156 Product Usage: For in vitro diagnostic use only. For the quantitative
Ortho-Clinical Diagnostics recalls VITROS NT-proBNP Reagent (Cat No. 6802156) due to potential biased results at low biotin concentrations. This affects in vitro diagnostic testing for heart failure and cardiac risk assessment.
Ortho-Clinical DiagnosticsNov 1, 2018 - UnratedMedical device
Clark Laboratories, Inc. (dba,Trinity Biotech USA) recalls ultra2 Genesys Variants Analyzer, REF 03-01-0045 intended to be used with automated high performance liquid
Trinity Biotech USA recalls Ultra2 Genesys Variants Analyzer (REF 03-01-0045) due to lack of 510K clearance. This device is for in vitro diagnostics and requires regulatory approval before use.
Trinity Biotech USANov 1, 2018 - Lower riskDrug
Bound Tree Medical, LLC recalls Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep
Bound Tree Medical recalls Curaplex Epi Safe Kit (Rx Only) due to incorrect expiration date labeling and missing 510(k) clearance on the syringe. Affected units expire May 2019 but labeled as May 2018.
Bound Tree MedicalNov 1, 2018
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,513 recalls tracked · 71,991 explained in plain English · 10,968 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.