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
34,894 found- Stop using nowFood
Ahold Usa recalls Ahold-Own Brands Whole Kernel Sweet Corn, 16 oz. Plastic Bag : Stop & Shop Brand Frozen Whole Kernel Sweet Corn, 16 oz.
Ahold recalls frozen whole kernel sweet corn products due to Listeria Monocytogenes detected in retail samples. Consumers should check product labels for affected brands and UPCs.
AholdNov 14, 2017 - Stop using nowConsumer product
Tech Drift Recalls Self-Balancing Scooters/Hoverboards Due to Fire and Explosion Hazards
Tech Drift recalls self-balancing scooters and hoverboards due to lithium-ion battery overheating risks. Products may smoke, catch fire, or explode. Return for free UL2272-certified replacement.
Tech DriftNov 14, 2017 - Stop using nowConsumer product
Sonic Smart Wheels Self-Balancing Scooters/Hoverboards Recalled by Dollar Mania Due to Explosion and Fire Hazards
Dollar Mania recalls Sonic Smart Wheels self-balancing scooters/hoverboards with model S-01 or SBW666SL due to lithium-ion battery overheating risks. Consumers must stop using and return for free UL2272-certified replacement.
Dollar ManiaNov 14, 2017 - Stop using nowConsumer product
Smart Balance Wheel Self-Balancing Scooters/Hoverboards Recalled by Salvage World Due to Explosion and Fire Hazards
Salvage World recalls Smart Balance Wheel hoverboards due to lithium-ion battery overheating risks. Stop using immediately to avoid fire or explosion.
Salvage WorldNov 14, 2017 - Stop using nowConsumer product
iLive Self-Balancing Scooters/Hoverboards Recalled by Digital Products Due to Fire Hazard
iLive self-balancing scooters/hoverboards with model numbers GSB56BC, GSB56RC, GSB65BUC, GSB56WC, and GSB56GDC are recalled due to fire risk from lithium-ion batteries. Consumers must stop using and get a free replacement.
iLiveNov 14, 2017 - Stop using nowConsumer product
iHoverspeed Self-Balancing Scooters/Hoverboards Recalled by Simplified Wireless Due to Fire Hazard
iHoverspeed self-balancing scooters are recalled due to lithium-ion battery overheating risks. Stop using immediately and contact Simplified Wireless for a free replacement.
iHoverspeedNov 14, 2017 - Stop using nowConsumer product
Go Wheels Self-Balancing Scooters/Hoverboards Recalled by Four Star Imports Due to Fire and Explosion Hazards; Sold Exclusively at Village Mart
Go Wheels self-balancing scooters/hoverboards with lithium-ion batteries may overheat and catch fire. Return to Four Star Imports for free UL2272-certified replacement.
Go WheelsNov 14, 2017 - Stop using nowConsumer product
Drone Nerds Recalls Self-Balancing Scooters/Hoverboards Due to Fire and Explosion Hazards
Drone Nerds recalls certain self-balancing scooters/hover: lithium-ion batteries can overheat, causing smoking, fire, or explosion. Stop using immediately and get a refund or store credit.
Drone NerdsNov 14, 2017 - Use cautionMeat & poultry
Pride of Iowa Sandwiches, Inc. Recalls Chicken, Pork and Beef Products Produced Without Benefit of Inspection
USDA FSIS recalls 231 pounds of un-inspected chicken, pork, and beef wraps produced without federal inspection. Consumers urged not to eat these products.
Pride of IowaNov 13, 2017 - Use cautionVehicle
PLEASANT VALLEY MYPOD TRAVEL TRAILER (2017) recall — Equipment
Pleasant Valley is recalling 2017-2018 MyPod travel trailers with Kidde 210D fire extinguishers that may become clogged or detach, increasing fire injury risk. Owners must get a replacement extinguisher free.
Pleasant ValleyNov 13, 2017 - Use cautionMedical device
Lifeline Systems Company recalls HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator.
Lifeline Systems recalls Model FD100 HomeSafe AutoAlert Pendants with specific reference numbers due to a programming error that may render fall detection inoperable.
Lifeline SystemsNov 13, 2017 - Lower riskMedical device
Cyberonics, Inc recalls VNS Therapy Programmer, Model 3000, v1.0 System
Cyberonics recalls Model 3000 v1.0 VNS Therapy Programmers with specific serial numbers due to potential programming errors that could cause incorrect stimulation levels or no therapy delivery.
CyberonicsNov 13, 2017 - Lower riskMedical device
Amendia, Inc dba Spinal Elements recalls Piranha Screw 4.0 x 12mm, used in Piranha Surgical Plate System The Piranha Surgical Plate System is intended to
Spinal Elements recalls Piranha Screw 4.0 x 12mm used in surgical plates. Some screws marked as 12mm actually measure 14mm, risking incorrect spinal fixation. Affected patients should contact for details.
Spinal ElementsNov 13, 2017 - Use cautionMedical device
Smiths Medical ASD Inc. recalls Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps are indicated for the following uses: 1)
Smiths Medical recalls Medfusion Syringe Pump 3010 Series models that may misidentify loaded medication syringes, causing incomplete programming. Affected units include specific model numbers and product codes.
Smiths MedicalNov 13, 2017 - UnratedDrug
Elite Laboratories Inc. recalls Isradapine Capsules USP 2.5 mg, 100-count bottles, Rx only, Manufactured by: Elite Laboratories, Inc. Northvale, NJ
Elite Laboratories recalls Isradapine Capsules USP 2.5 mg 100-count bottles (Rx only) due to failed impurities/degradation specifications. No remedy stated in official notice.
Elite LaboratoriesNov 13, 2017 - Stop using nowDrug
Fresenius Medical Care Renal Therapies Group, LLC recalls 0.9% Sodium Chloride Injection, USP, 1000 mL, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC
Fresenius Medical Care recalls 1000 mL bags of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility.
Fresenius Medical CareNov 13, 2017 - Stop using nowFood
Arise Gluten Free Bakery recalls Arise Gluten Free Bakery Wild Yeast Sourdough; NET WEIGHT 24 OZ (680 grams) UPC 095225600005
Arise Gluten Free Bakery recalls Wild Yeast Sourdough bread due to glass shards. Check lot 1310187 and UPC 095225600005.
Arise Gluten Free BakeryNov 13, 2017 - Use cautionVehicle
ASTON MARTIN DB9 (2015) recall — Power Train
Aston Martin recalls 2015 DB9 vehicles with potential transmission park pawl failure causing unexpected rolling on slopes. Owners must update TCM software by February 2018 to prevent crashes.
Aston MartinNov 12, 2017 - Use cautionVehicle
INTERNATIONAL LT (2018) recall — Equipment
Navistar recalls certain 2018 LT trucks with potentially clogged Kidde fire extinguishers that could fail during a fire, increasing injury risk. Owners must contact Kidde for a free replacement by February 9, 2018.
NavistarNov 12, 2017 - UnratedDrug
Renaissance Lakewood, LLC recalls Fluconazole Injection, USP, 2 mg/mL, a) 50 mL (NDC 336000-261-10) and b) 100 mL (NDC 33600-002-10), Rx Only,
Renaissance Lakewood recalls fluconazole injection (2 mg/mL) due to superpotent risk. Rx-only products with specific NDC numbers are affected. Contact for details.
Renaissance LakewoodNov 11, 2017 - Use cautionFood
Bush Brothers & Co recalls BUSH'S BEST¿ Homestyle TANGY SAUCE WITH BACON & BROWN SUGAR BAKED BEANS 55 OZ (3 LB 7 OZ) 1.56 kg BUSH BROTHERS &
Bush Brothers recalls specific lots of Homestyle Tangy Sauce with Bacon & Brown Sugar Baked Beans due to swollen cans. Check your pantry.
Bush's BestNov 11, 2017 - Stop using nowVehicle
NISSAN VERSA (2012) recall — Suspension
Nissan recalls certain 2012 Versa Hatchbacks due to corroded front coil springs that may fracture and puncture tires, increasing crash risk. Free repair available.
NissanNov 10, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100, Catalog #s: 800-3046, 800-3047, 800-3052,
Beckman Coulter recalls iQ200 Series Urine Microscopy Analyzers with NFT-2100 barcode readers that may fail to read urine sample barcodes, causing incorrect results that could delay treatment for conditions like hematuria.
Beckman CoulterNov 10, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls BARD(R) CRITICORE(R) MONITOR, Model: 000002N Series The CritiCore(R) Automated Urine Output and Temperature Monitor is
C.R. Bard recalls CritiCore monitors with serial numbers listed that may have urine output and temperature measurement fluctuations, causing potential inaccuracies in patient monitoring.
C.R. BardNov 10, 2017 - Use cautionMedical device
NxStage Medical, Inc. recalls NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with NxStage System One
NxStage recalls premixed dialysate for hemodialysis due to risk of health issues if different fluid formulations are used simultaneously during treatment. The original labeling did not warn against mixing dialysate formulations.
NxStageNov 10, 2017 - Lower riskMedical device
Wiener Laboratories recalls Wiener Lab CHAGATEST ELISA RECOMBINANTE V. 3.0 Diagnosis of Chagas disease.
Wiener Laboratories recalls CHAGATEST ELISA Recombinant V 3.: Product may expire before indicated date. No remedy specified in recall notice.
Wiener LaboratoriesNov 10, 2017 - Stop using nowMedical device
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and
Moog Medical recalls Curlin Infusion Administration Sets with particulate in the spike, which could cause blockages or infections during IV use. Affected units include specific model and serial numbers.
Moog MedicalNov 10, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls CritiCore Automated Urine Output and Temperature Monitor
C.R. Bard recalls CritiCore Automated Urine Output and Temperature Monitors with potential urine output and temperature measurement errors and false alarms. Affected models include DYZIAA003, DYAPAA017, and other serial numbers listed in the recall.
C.R. BardNov 10, 2017 - Use cautionMedical device
Philips Medical Systems (Cleveland) Inc recalls Ingenuity Core 128, (Code 728323) Intended to produce images of the head and body by computer reconstruction of x-ray
Philips recalls certain Ingenuity Core 128 x-ray scanners due to potential fastener issues that could cause parts to become loose during use. Affected units have specific serial numbers and codes.
Philips Medical SystemsNov 10, 2017 - Stop using nowDrug
Baxter Healthcare Corporation recalls Nexterone (amiodarone HCl) Premixed Injection, 150mg/100mL, 100-mL bag, Rx Only, Sterile, Baxter Healthcare
Baxter Healthcare recalls Nexterone amiodarone injections due to polyethylene particles in the packaging. This could cause serious injury if injected. Affected units have specific NDC and lot numbers.
Baxter HealthcareNov 10, 2017
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