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
34,960 found- Use cautionVehicle
FOREST RIVER CHEROKEE (2020) recall — Equipment
Forest River is recalling 2020 Cherokee trailers with incorrect weight placards that could cause trailer overload and loss of control. Owners should contact customer service for free replacement placards.
Forest RiverJun 14, 2019 - Lower riskMedical device
Wilson-Cook Medical Inc. recalls Acuject Variable Injection Needle
Wilson-Cook Medical recalls Acuject Variable Injection Needles with potential occlusion risk. Learn about affected lots and safety steps.
Wilson-Cook MedicalJun 14, 2019 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F
Bard recalls EQUISTREAM XK Long-Term Hemodialysis Catheters with incorrect peel-apart introducer sheath. This may cause complications during dialysis procedures. Affected units have specific model and serial numbers.
BardJun 14, 2019 - Stop using nowMedical device
CooperSurgical, Inc. recalls Advincula Delineator with Ultem Plastic Soft Cup size 3.0 cm; Part No. AD750SC-KE30 The Advincula Delineator Uterine
CooperSurgical recalls Advincula Delineator size 3.0 cm soft cups due to potential cracking from excessive compressions, which could cause lacerations during uterine procedures.
CooperSurgicalJun 14, 2019 - Lower riskMedical device
Stanley Security Solutions Inc recalls STANLEY Healthcare Arial 54315 Network Manager
Stanley Healthcare recalls Arial 54315 Network Manager units with specific serial numbers due to reported outages in nurse call systems.
Stanley HealthcareJun 14, 2019 - Use cautionMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo Capiox NX19 Oxygenator With Reservoir (East Orientation) P/N: 3CX*NX19RE
Terumo recalls oxygenator model 3CX*NX19RE with possible non-functioning thermistor that could cause oxygen delivery issues. Affected units sold in 2017 with lot number WP17.
TerumoJun 14, 2019 - Lower riskMedical device
TELEFLEX-MORRISVILLE recalls Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
Teleflex-Morrisville recalls Babi.Plus 12.5 cm H2O Pressure Relief Manifold (Catalog # 2691) due to potential venting of gas below stated pressure levels when used with ventilators.
Teleflex-MorrisvilleJun 14, 2019 - UnratedDrug
Golden State Medical Supply Inc. recalls Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10
Golden State Medical Supply recalls 50mg Losartan Potassium tablets due to impurity detected in manufacturing. Affected lots may pose health risks; contact for details.
Golden State Medical SupplyJun 14, 2019 - UnratedFood
Frito-Lay, Inc. recalls Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt. 7 3/4 OZ. UPC Code 2840063242
Frito-Lay recalls Lay' Lightly Salted Barbecue Flavored Potato Chips with undeclared milk. Check UPC 2840063242 for affected items. No remedy provided in official notice.
Frito-LayJun 14, 2019 - Stop using nowFood
California Shellfish, Inc. dba Hallmark Fisheries recalls Ocean Supreme and Yaquina Bay IQF shrimp meat, product of USA wild caught, cooked and peeled, 5 lb. bag, 4/5 lb. bags
Hallmark Fisheries recalls Ocean Supreme and Yaquina Bay IQF shrimp meat due to foreign object in packaging. Consumers should stop using affected products immediately.
Hallmark FisheriesJun 14, 2019 - Stop using nowFood
Mizkan America, Inc. - Corporate recalls Ragu Old World Style Sauce Flavored with Meat 66oz retail size sold in plastic jar
Mizkan America recalls Ragu Old World Style Sauce Flavored with Meat (66oz) due to foreign material. Check your jars for the specific best use by date.
RaguJun 14, 2019 - Stop using nowFood
Sprout's Farmers Market recalls Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb), 453 g, Manufactured exclusively for Sprouts Farmers
Sprouts Farmers Market recalls 16 oz Cut Leaf Spinach due to Listeria monocytogenes. Check your product for the specific use-by date and UPC.
Sprouts Farmers MarketJun 14, 2019 - Use cautionVehicle
JEEP CHEROKEE (2014) recall — Power Train
Chrysler recalls certain 2014 Jeep Cherokees with 3.2L engines due to potential unintended neutral shift causing loss of drive and crash risk. Owners must contact customer service for free software update.
ChryslerJun 13, 2019 - Use cautionVehicle
ROADTREK CS ADVENTUROUS (2018) recall — Seats
Erwin Hymer recalls 2:2013-2019 Roadtrek CS Adventurous motorhomes with second-row captain seats that may not protect occupants in crashes. Free repairs to install seatbelt labels.
Erwin HymerJun 13, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Tires
Chrysler recalls 2019 RAM 1500 trucks with potentially incorrect spare tire size that could lead to crash risk if inflated improperly. Owners must get correct spare tire installed free.
ChryslerJun 13, 2019 - Use cautionVehicle
JEEP CHEROKEE (2019) recall — Air Bags
Chrysler recalls certain 2019 Jeep Cherokees due to potential air bag deployment failure in crashes, increasing injury risk. Owners must have sensors replaced free by dealers.
ChryslerJun 13, 2019 - Lower riskMedical device
SpineFrontier, Inc. recalls A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
SpineFrontier recalls A-CIFT SoloFuse Fixed Angle Driver Model 13-32101-01 (Lot EC20) due to potential binding when advancing intervertebral body fixation screws. Affected users should contact SpineFrontier for details.
SpineFrontierJun 13, 2019 - Lower riskDrug
Baxter Healthcare Corporation recalls Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation
Baxter Healthcare recalls 250mL Sevoflurane inhalation anesthetic bottles due to failed stability specifications. This could affect medication safety. Check your product details for recall.
Baxter HealthcareJun 13, 2019 - Lower riskDrug
B. Braun Medical Inc recalls Heparin Sodium 25,000 USP units per 250 mL (100 USP units per mL) in 5% Dextrose Injection, 250 mL EXCEL Container bag,
B. Braun Medical recalls heparin sodium 25,000 USP units per 250mL in 5% dextrose injection due to subpotent drug levels. This may cause ineffective blood thinning during medical procedures.
B. Braun MedicalJun 13, 2019 - Stop using nowFood
B.C. Frozen Foods recalls Gordon CHOICE Whole Strawberries; 5lb bags; UPC Code 93901 24463 5
B.C. Frozen Foods recalls Gordon CHOICE 5lb bags of whole strawberries due to potential norovirus contamination. Check your UPC and lot numbers.
Gordon CHOICEJun 13, 2019 - Stop using nowFood
Oregon Potato Company recalls Frozen whole Red Raspberries; packed in a 12 oz. polyethylene bag; UPC: 0 70552 30501 4. The label is read in parts:
WinCo Foods recalls frozen whole red raspberries due to potential Norovirus contamination. Check your freezer for the specific UPC and best-by date.
WinCo FoodsJun 13, 2019 - Stop using nowConsumer product
American Honda Recalls Recreational Off-Highway Vehicles Due to Crash and Injury Hazards (Recall Alert)
Honda recalls 2016-2019 Pioneer 1000 side-by-side vehicles due to throttle pedal sticking, which can cause crashes and injuries. Owners must stop using and contact a dealer for free repair.
HondaJun 13, 2019 - Lower riskMeat & poultry
Pasture Raised Foods, LLC Recalls Raw Whole Poultry Products Produced Without Benefit of Inspection
Pasture Raised Foods LLC recalls frozen raw whole poultry products made without federal inspection. Consumers are urged not to consume these items, which lack a USDA mark of inspection but have an unapproved label.
Greener Pastures ChickenJun 12, 2019 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Engine And Engine Cooling
Daimler Trucks North America recalls 2020-2021 Thomas Built Saf-T-Liner C2 school buses with Detroit Diesel engines due to loose fan hub bolts that could cause engine failure and injury risk.
Thomas BuiltJun 12, 2019 - Lower riskMedical device
Beckman Coulter Inc. recalls SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250); Catalog No. 475012 - Product Usage: BARB reagent, in conjunction
Beckman Coulter recalls SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250) due to potential false positive or negative urine test results from cross-reactivity in certain compounds. Affected units include specific catalog numbers and lot numbers.
Beckman CoulterJun 12, 2019 - Use cautionMedical device
ZOLL Medical Corporation recalls ZOLL AED PRO Automated External Defibrillator Product Usage: The AED PRO unit is intended to defibrillate victims of
ZOLL Medical Corporation recalls AED PRO devices that may fail to deliver energy to patients during cardiac arrest. Affected units have specific serial numbers and part numbers listed. Users should stop using and contact ZOLL for replacement.
ZOLLJun 12, 2019 - Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes, Catalog Number 367886
Becton Dickinson recalls BD Vacutainer Lithium Heparin blood collection tubes due to false carboxyhemoglobin results when used with IL GEM 4000 blood gas analyzers. Affected tubes have catalog number 367886.
Becton DickinsonJun 12, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dTC, Model Number 7413078
Siemens recalls specific AXIOM Artis dTC X-ray machines (model 7413078) due to power supply tolerance issues that can cause X-ray tube failure during procedures. Affected units have listed serial numbers.
SiemensJun 12, 2019 - Use cautionDrug
InvaGen Pharmaceuticals, Inc. recalls Testosterone Topical Solution 30mg of testosterone per pump actuation * each actuation delivers 1.5 mL of solution
InvaGen recalls Testosterone Topical Solution due to defective containers that may deliver incorrect doses. Check lot numbers GH80480 and GH80481.
InvaGen PharmaceuticalsJun 12, 2019 - Stop using nowDrug
Infusion Options, Inc. recalls INJECTAFER 720 MG in 100 ml NS IVPB; INJECTAFER 210 MG in 100 ml NS IVPB, Rx Only, Infusion Options, Inc. 5924 13the
Infusion Options recalls Injectaferr 720 mg and 210 mg IV bags due to lack of sterility assurance. Check your lots immediately.
InjectaferrJun 12, 2019
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