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
35,025 found- Stop using nowFood
TESOROS TRADING CO. recalls Trader Joe's Lightly Salted Edamame: Fully Cooked Soybeans in Pod. Keep Frozen NET WT 16 oz. (1 lb.) 454 g UPC: 0051
Trader Joe's Lightly Salted Edamame (16 oz) recalled due to Listeria monocytogenes contamination. Consumers should stop using and discard affected products.
TESOROS TRADING CO.Dec 16, 2020 - Stop using nowConsumer product
LG Energy Solution Michigan Recalls Home Energy Storage Batteries Due to Fire Hazard
LG Energy Solution recalls RESU 10H home energy storage batteries due to fire risk from overheating. Owners must contact for free replacement or modifications to prevent fire.
LG Energy SolutionDec 16, 2020 - Stop using nowConsumer product
Graco Recalls Inclined Sleeper Accessory Included with Four Models of Playards to Prevent Risk of Suffocation
Graco recalls inclined sleeper accessories with four Playard models due to reported infant suffocation risks from rolling. Consumers should stop using the accessory and get a refund for the recalled part.
GracoDec 16, 2020 - Use cautionConsumer product
Cycling Sports Group Recalls Cannondale Canvas NEO Bicycles Due to Fall Hazard
Cycling Sports Group recalls all Cannondale Canvas NEO e-bikes with electric motors due to front fender detachment risk causing falls. Consumers must stop using until fender is removed and get free repair.
Cycling Sports GroupDec 16, 2020 - Stop using nowConsumer product
Camp Chef Recalls Portable Gas Stoves Due to Fire Hazard
Camp Chef recalls portable stoves with model MS4:0A, MSHP, MSGG and gas regulators dated 1923-2030 due to fire risk from gas leaks. Consumers must stop using and get free regulator replacements.
Camp ChefDec 16, 2020 - Stop using nowConsumer product
BRP Recalls Can-Am Screw Jacks Due to Crush Hazard
BRP Can: Can-Am Off-Road screw jacks sold for Maverick X3 vehicles recall due to crush hazard from vehicle collapse. Get refund by contacting dealer.
BRP Can-AmDec 16, 2020 - Use cautionVehicle
ROSENBAUER COMMANDER (2018) recall — Electrical System
Rosenbauer recalls 2018-2021 Commander vehicles with faulty LCD displays that may lock up, delaying emergency efforts and increasing injury risk. Owners can get free repairs or replacements.
RosenbauerDec 15, 2020 - Use cautionVehicle
VOLVO VNR (2021) recall — Service Brakes, Hydraulic
Volvo recalls 2021 VNR trucks where park brakes might activate unexpectedly, risking loss of vehicle control. Owners must have brakes inspected by dealers by January 31, 2021.
Volvo TrucksDec 15, 2020 - Use cautionVehicle
JAYCO GREYHAWK (2020) recall — Equipment
Jayco is recalling 2020-2021 Greyhawk motorhomes due to hydraulic pump and reservoir mounting brackets that may detach, risking leaks and crashes. Owners must contact Jayco for free bracket installation.
JaycoDec 15, 2020 - Use cautionVehicle
DUCATI SCRAMBLER (2020) recall — Electrical System
Ducati recalls 2018-2021 Scrambler 1100 motorcycles with potential electrical short-circuit fire risk. Owners must have cable guide and self-locking cable tie installed by dealers.
DucatiDec 15, 2020 - Lower riskMedical device
Boston Scientific Corporation recalls ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to facilitate guide catheter removal after the Boston
Boston Scientific recalls Model 7060 ACUITY cutters that may not have been properly sterilized, posing a risk of infection. Affected units were distributed in the US with specific GTIN and lot numbers.
Boston ScientificDec 15, 2020 - Stop using nowMedical device
Wahl Clipper Corp recalls WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
Wahl recalls 4212 heated massagers due to fire risk from overheating connections. All units are affected; stop using immediately to prevent fire.
WahlDec 15, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls PORTEX Bivona Cuffless Neonatal/Pediatric FlexTend Tracheostomy Tube, REF 60PFSS45
Smiths Medical recalls specific FlexTend Tracheostomy Tubes due to potential incorrect packaging with a V-neck flange instead of straight flange. Affected units may need verification.
Smiths MedicalDec 15, 2020 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls Pinnacle Cups, Part numbers 121701048 121701050 121701052 121701054 121701056 121701058 121701060 121701062 121711048
DePuy Orthopaedics is a leading manufacturer of surgical implants and medical devices for orthopedic procedures. Their products include joint replacements, spinal implants, and trauma devices.
DePuy OrthopaedicsDec 15, 2020 - Use cautionMedical device
Penumbra Inc. recalls Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing REF 5MAXJET7KIT The Penumbra JET 7
Penumbra recalls JET 7 Reperfusion Catheter kits due to potential distal tip damage during use that could cause vessel injury or death if contrast injection pressure is applied.
PenumbraDec 15, 2020 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) - IVD quantitatively measures total protein (TP)
Ortho Clinical Diagnostics recalls VITROS XT ALB-TP Slides due to potential false protein results. Affected units include all current, future, and past lots of product code 6844293.
Ortho Clinical DiagnosticsDec 15, 2020 - Lower riskMedical device
Brainreader ApS recalls Neuroreader Medical Image Processing Software - Product Usage: intended to automate the current manual process of
Brainreader recalls Neuroreader software version 2.4 due to FDA-cleared database mismatch. Users may face incorrect medical analysis results from outdated reference norms.
BrainreaderDec 14, 2020 - Lower riskMedical device
Phadia US Inc recalls EliA dsDNA Well - Product Usage: intended for the In-Vitro quantitative measurement of IgG antibodies directed to dsDNA
Phadia recalls specific EliA dsDNA Well kits for potential false positive results in lupus testing. Affected kits may give inaccurate results for systemic lupus diagnosis.
PhadiaDec 14, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040 /Venovo 9F 14/40/1200mm OUS; VENEL14060
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 9F models with serial numbers starting with ANE... due to reports of stent not expanding immediately after deployment and remaining connected to delivery system. Affected units include specific model codes and serial numbers listed in the recall notice.
Bard Peripheral Vascular IncDec 14, 2020 - Lower riskMedical device
K2M, Inc recalls Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026), component of YUKON Spinal System
K2M recalls Yukon Polyaxial Screw Size 4.0x26mm (catalog 7601-04026) due to incorrect laser marking. This may lead to improper spinal surgery use. Affected units have lot number KRBX.
K2MDec 14, 2020 - Use cautionMedical device
Prytime Medical Devices, Inc. recalls PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA,
Prytime Medical recalls Reboa Catheter Introducer Kit (KT1835C) due to possible 21G needle instead of 18G. Using this wrong needle may cause procedure delays or injury during vascular access.
Prytime MedicalDec 14, 2020 - Lower riskMedical device
Integra LifeSciences Corp. recalls Bactiseal Ventricular Catheter with Bactiseal Shunt System - Product Usage: use in the treatment of hydrocephalus as a
Integra LifeSciences recalls Bactise:al Ventricular Catheter (823073) mislabeled as Bactiseal Endoscopic Ventricular Catheter (823087). This could lead to incorrect use in hydrocephalus treatment. Affected units: Lot 4178253, exp. Nov 2019.
Integra LifeSciencesDec 14, 2020 - Lower riskDrug
CIPLA recalls Azacitidine for Injection 100 mg/vial For Subcutaneous and Intravenous Use Only Single-Dose Vial Manufactured by Shilpa
Cipla recalls Azacitidine 100 mg vials due to potential sterility issues from improper sealing during manufacturing. Affected vials have specific lot numbers and distribution details. Consumers should contact Cipla for guidance.
CiplaDec 14, 2020 - Lower riskDrug
SCA Pharmaceuticals, Inc. recalls Vasopressin 20 Units added to 0.9% Sodium Chloride 100 mL Rx Only, Single Dose Container, SCA Pharmaceuticals 8821
SCA Pharmaceuticals recalls Vasopressin 20 Units in 0.9% Sodium Chloride 100 mL containers due to subpotent drug. Affected lots have specific barcodes and expiration dates.
SCA PharmaceuticalsDec 14, 2020 - Use cautionVehicle
JEEP GRAND CHEROKEE (2019) recall — Engine And Engine Cooling
Chrysler is recalling 2014-2019 Jeep Grand Cherokees with 3.0L EcoDiesel engines due to a fire risk from potential combustion in the intake manifold.
FCADec 11, 2020 - Use cautionVehicle
TOYOTA RAV4 PRIME (2021) recall — Exterior Lighting
Toyota recalls 2021 RAV4 Prime vehicles with improperly closed headlight aiming caps that can cause glare, reducing visibility and increasing crash risk. Owners must have caps closed by dealers.
ToyotaDec 11, 2020 - Use cautionVehicle
BMW Z4 (2020) recall — Fuel System, Gasoline
BMW is recalling certain 2020-2021 Z4 vehicles due to a potential fuel leak from a faulty weld, which could cause fire if an ignition source is present. Owners must have the fuel tank replaced at no cost.
BMWDec 11, 2020 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls FUJIFILM Synapse PACS Software: versions 7.0.0 and 7.0.1 - Product Usage: intended for use as a web based application
Fujifilm recalls PACS software versions 7.0.0 and 7.0.1 due to clinical reporting errors when ventricular traces are changed by different users. Affected users should check their software version and contact Fujifilm for updates.
FujifilmDec 11, 2020 - Lower riskMedical device
Steris Corporation recalls Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for use in the cleaning and intermediate
Steris Corporation is a global leader in medical device manufacturing and healthcare solutions. We provide innovative products and services to improve patient care and operational efficiency in healthcare settings.
SterisDec 11, 2020 - Lower riskMedical device
Baxter Healthcare Corporation recalls VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal
Baxter Healthcare recalls VERITAS Collagen Matrix 12x25 cm patches that may have undersized width dimensions. This affects pelvic floor reconstruction and rectal prolapse repair products with specific lot numbers and expiration dates.
Baxter HealthcareDec 11, 2020
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,613 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.