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
35,004 found- Use cautionMedical device
James Leckey Design Ltd recalls Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable
James Leckey Design recalls Firefly Splashy Bathseats with broken latches that could cause falls. Affected units have specific serial numbers or codes. Stop using immediately to prevent injury.
James Leckey DesignFeb 18, 2020 - Lower riskMedical device
Randox Laboratories Ltd. recalls Chemistry QC Premium Plus, Cat. No. LAL4213, GTIN 05055273209006 - Product Usage: This product is intended for in vitro
Randox recalls Chemistry QC Premium Plus (LAL4213) due to incorrect sodium control target values for in vitro diagnostics. This may affect lab accuracy in diagnostic testing.
RandoxFeb 18, 2020 - Lower riskMedical device
Microbiologics Inc recalls QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro
Microbiologics recalls QC sets and KWIK-STIK AST-GP kits that may return incorrect bacterial susceptibility results, affecting lab testing accuracy.
MicrobiologicsFeb 18, 2020 - Use cautionMedical device
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and
Avid Medical recalls custom surgical procedure trays containing non-sterile surgical gowns that could cause infections during surgery. Affected items include specific model numbers and lot numbers sold between 2020-2022.
Avid MedicalFeb 18, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls MEVATRON M2/Primus Mid-Energy Model #01940035, MEVATRON PRIMART #05500371, MEVATRON KD-2 #08515520, MEVATRON KD2
Siemens Medical recalls specific MEVATRON radiation therapy models due to potential 10-20% overdose risk from dose monitoring system failures.
Siemens MedicalFeb 18, 2020 - Lower riskFood
Saratoga Potato Chips LLC recalls Kroger Sweet & Mesquite BBQ potato chips -17 oz. UPC: 0-11110-03201-0
Kroger Sweet & Mesquite BBQ potato chips (17 oz, UPC 0-11110-03201-0) recalled due to undeclared milk. Consumers should check labels and contact retailer for details.
Saratoga Potato Chips LLCFeb 18, 2020 - Lower riskFood
Paleonola Llc recalls Paleonola Grain Free Granola; Pumpkin Pie; packaged in 10oz stand-up pouches; UPC 013964497137
Paleonola recalls 10oz grain-free granola and pumpkin pie pouches potentially contaminated with unapproved herbicide haloxyfop. Consumers should check UPC 013964497137 and best by dates for affected products.
PaleonolaFeb 18, 2020 - Use cautionVehicle
JAYCO SEISMIC (2014) recall — Suspension
Jayco recalls 2013-2015 Fifth Wheel Seismic and Pinnacle trailers with 6,000lb axles instead of 7,000lb. This may cause trailer overload and loss of vehicle control, increasing crash risk. Owners should contact Jayco for free axle replacement.
JaycoFeb 17, 2020 - Use cautionVehicle
BENTLEY BENTAYGA (2019) recall — Air Bags
Bentley is recalling 2018-2020 Bentayga vehicles with side curtain air bags that may not inflate properly in crashes, increasing injury risk. Owners can get free replacements.
BentleyFeb 17, 2020 - Lower riskMedical device
Advanced Bionics, LLC recalls AB HiResolution Bionic Ear System, HiRes Ultra CI, MS Electrode - Product Usage: The device is intended to restore a
Advanced Bionics recalls HiResolution Bionic Ear Systems (model CI 1600 04/05) due to hearing performance issues from body fluids entering the device. Affected units sold with lot numbers 1000000-1999999.
Advanced Bion: Bionic Ear SystemFeb 17, 2020 - Lower riskMedical device
Biomet, Inc. recalls Comprehensive Shoulder System Mini Humeral Stem 9mm,, Model No. 113629 - Product Usage: The intended use of the
Biomet recalls 9mm Shoulder Mini Humeral Stem (Model 11362: Lot 659260) due to misidentification as 15mm. This could lead to improper joint fitting and potential complications during surgery.
BiometFeb 17, 2020 - Lower riskMedical device
Beckman Coulter, Inc. recalls iChemVELOCITY Strips, Catalog 800-7212
Beckman Coulter recalls iChemVELOCITY Strips (Lot 7212269M) due to Leukocyte and Compensation pads being switched in some vials. Affected users should contact for details.
Beckman CoulterFeb 17, 2020 - Lower riskDrug
Strides Pharma Science Limited recalls Potassium Chloride Extended-Release Tablets USP, 10mEq (750mg), 1000-count bottle, Rx only, Manufactured by: Strides
Strides Pharma recalls Potassium Chloride Extended-Release Tablets with oversized tablets in specific lots. These tablets may cause injury if taken. Check your NDC and lot numbers for affected products.
StridesFeb 17, 2020 - Use cautionVehicle
KIA SEDONA (2010) recall — Electrical System
Kia recalls 2010 Sedona vehicles with potential ABS module electrical short causing engine fire. Owners must have relay installed by dealer to prevent fire risk.
KiaFeb 14, 2020 - Use cautionMedical device
Hill-Rom Inc. recalls NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is
Hill-Rom recalls NaviCare Patient Safety Software versions 3.5.400-3.9.300 due to potential failure to monitor patient bed exits. Affected units include specific bed models with these software versions.
Hill-RomFeb 14, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Ethyl Alcohol, Test Code ETOH, Siemens Material Number (SMN) 11097501, UDI 00630414596112. The product is
Siemens Healthcare recalls Atellica CH Ethyl Alcohol test kits with potential positive bias in patient results and QC tests within 10-day calibration intervals. Affected lots include 190133, 190222, 100066, 100168.
Siemens HealthcareFeb 14, 2020 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Artis Q.zen Biplane, Model No. 10848355 Artis Q.zen Ceiling, Model No. 10848354 Artis Q.zen Floor, Model No. 10848353
Siemens recalls Artis Q.zen Biplane, Ceiling, and Floor models due to a software issue that could block stand and table movements. Affected units have specific serial numbers listed in the recall notice.
SiemensFeb 14, 2020 - Lower riskMedical device
ICU Medical, Inc. recalls The Cogent Hemodynamic Monitoring System. REF58400-000, GTIN 00840619099459; REF 58400-000R, GTIN 0087709094314; REF
ICU Medical recalls Cogent Hemodynamic Monitoring System with software issues causing patient ID and information not to be stored. Affected units include specific model numbers and software versions.
ICU MedicalFeb 14, 2020 - Lower riskMedical device
Micro Therapeutics Inc, Dba Ev3 Neurovascular recalls ev3 Pipeline Flex Embolization Device. For neurological endovascular use.
Ev3 Neurovascular recalls certain Pipeline Flex Embolization Devices for neurological endovascular use due to potential fracture at the distal section during implantation, which could cause unintended separation of the device in the patient.
Ev3 NeurovascularFeb 14, 2020 - UnratedDrug
AAA Pharmaceutical, Inc. recalls Discount Drug Mart, Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg /Antihistamine, Indoor/Outdoor
AAA Pharma recalls Discount Drug Mart Allergy Relief tablets due to incorrect or missing lot and expiration dates. Check your bottles now.
Discount Drug MartFeb 14, 2020 - Lower riskFood
Custom Foods LLC recalls Sticky Fingers Bakeries Gluten-Free Scones, Quick & Easy Mix, Meyer Lemon; Net Wt. 14 oz. (0.875 LBS) 396.9g. In
Custom Foods LLC recalls Gluten-Free Scones with wheat in ingredient list. Product may not be truly gluten-free. Consumers should check ingredient list for wheat flour.
Sticky Fingers BakeriesFeb 14, 2020 - Lower riskFood
CJ Foods Inc., A Division of CJ America recalls Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked Hokkien Noodles - Sweet & Tangy sauce with Bok choy and
Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked Hokkien Noodles was recalled due to undeclared peanuts on the label. The product contains peanuts but was packaged with a sleeve that left peanuts visible on the label.
Annie Chun'sFeb 14, 2020 - Use cautionVehicle
JAGUAR XF (2010) recall — Fuel System, Gasoline
Jaguar recalls 2010 XF vehicles with 4.2L engines due to potential fuel leaks near ignition sources that could cause fire. Owners must have fuel outlet flange replaced free of charge.
JaguarFeb 13, 2020 - Use cautionVehicle
RAM 1500 (2019) recall — Power Train
Chrysler recalls certain 2019 Ram 1500 trucks with a transfer case issue that may cause sudden power loss or loss of 'PARK' function. Owners must have the transfer case replaced free of charge.
ChryslerFeb 13, 2020 - Use cautionVehicle
BMW C 400 X (2019) recall — Vehicle Speed Control
BMW recalls 2019 C400X scooters due to water in throttle cable that can freeze, causing stuck throttle and crash risk. Free replacement of improved throttle cable.
BMWFeb 13, 2020 - Use cautionVehicle
JAGUAR I-PACE (2020) recall — Seats
Jaguar recalls one 2020 I-Pace vehicle due to potential seat frame weakness that could increase injury risk in crashes. Owners will receive free seat replacement.
JaguarFeb 13, 2020 - Use cautionVehicle
HEARTLAND PIONEER (2020) recall — Equipment
Heartland is recalling 2020 Pioneer fifth wheel trailers due to smoke detector placement in bedrooms that may not warn occupants during fires, increasing injury risk. Owners must contact Heartland for free relocation or additional detector installation.
HeartlandFeb 13, 2020 - Lower riskMedical device
NuVasive Inc recalls NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use
Recall of NuVasive MAGEC 2 spinal rods with specific lot numbers due to risk of internal component separation after implantation, potentially causing tissue discoloration.
NuVasiveFeb 13, 2020 - Lower riskMedical device
Merit Medical Systems, Inc. recalls DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System,
Merit Medical recalls vertebrae assembly products with incorrect 5-year expiration labels. These products may not function properly or require procedure rescheduling if used beyond their 2-year shelf life.
Merit MedicalFeb 13, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Chemistry Total Bilirubin_2 assay- SMN: 10341115 (40 mL) & 10341113 (70 mL). Product Usage: ADVIA TBIL_2 is for
Siemens Healthcare recalls ADVIA TBIL_2 bilirubin assay kits that may show false high results for patients on eltrombopag therapy. This could lead to incorrect liver treatment decisions. Affected kits have specific serial numbers.
Siemens HealthcareFeb 13, 2020
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.