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
34,959 found- Use cautionFood
Kwokcheng Enterprise, Inc. dba Fullei Fresh recalls Fullei Fresh brand Organic Mung Bean Sprouts in a 4 oz. clear plastic clamshell container
Fullei Fresh recalls organic mung bean sprouts from February 2019 with potential Listeria monocytogenes contamination. Consumers should check lot codes and dates for affected products.
Fullei FreshMar 8, 2019 - Stop using nowConsumer product
TJX Recalls Heating Pads Due to Fire and Burn Hazards; Sold Exclusively at T.J. Maxx and Marshalls Stores
T.J. Maxx and Marshalls sold Aroma Home USB heated pads that can overheat, causing fire or burns. Consumers must stop using and return for full refund.
Aroma HomeMar 8, 2019 - Use cautionVehicle
FIAT 500 (2018) recall — Power Train
DLT recalls certain Fiat 500 (2018) power train shifter shafts that may break while driving, increasing crash risk. Owners receive free replacement with updated shaft.
DLTMar 7, 2019 - Use cautionVehicle
WINNEBAGO FORZA (2019) recall — Structure
Winnebago recalls 2017-2019 Forza motorhomes where the storage compartment door may open while driving, risking crashes from other drivers swerving or objects falling.
WinnebagoMar 7, 2019 - Use cautionVehicle
BMW X5 (2019) recall — Fuel System, Other
BMW is recalling 2019 X5 vehicles with potential fuel leaks that could cause fire if near ignition sources. Owners must have fuel pumps replaced free by dealers.
BMWMar 7, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1600 Analyzer, Material Number 11066000
Siemens Healthcare recalls Atellica IM 1600 Analyzers with Material Number 11066000 due to software issues requiring an update. Affected units may need correction to prevent potential errors.
Siemens HealthcareMar 7, 2019 - Use cautionMedical device
Becton Dickinson & Company recalls BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
Becton Dickinson recalls BD Blood Collection Assembly with Male Luer Lock (Catalog MBC6010) due to risk of luer breaking, causing leaks or getting stuck in dialysis ports. Affected units have specific lot numbers. Patients may need re-cannulation.
Becton DickinsonMar 7, 2019 - Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Becton Dickinson recalls Eclipse blood collection needles (22Gx1.25) due to missing bevel causing blood leakage. Affected lots include 8207894, 9025826, 8354527, and 9010765.
Becton DickinsonMar 7, 2019 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Abbott Alinity ci-series System Control Module software version 2.5.1; LN 3R70-01 with the following hardware: Level
Abbott recalls Alinity ci-series System Control Module software version 2.5.1 (LN 3R70-01) due to potential performance issues. Affected units include specific hardware components for Alinity i and Alinity c analyzers.
AbbottMar 7, 2019 - Use cautionMedical device
Stryker Corporation recalls Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx,
Stryker recalls High Flow II Tube Set (REF 0620-040-660) due to consistent leaking and detachment from the PNEUMO SURE High Flow Insufflator, posing a risk of improper use during medical procedures.
StrykerMar 7, 2019 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the
BioFire Diagnostics recalls FilmArray BCID Panels that may cause false positive results for Enterobacteriaceae and E. coli when used with specific blood culture bottles. Affected units include certain model numbers and lots.
BioFire DiagnosticsMar 7, 2019 - Lower riskDrug
Medtech Products, Inc. recalls Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant
Medtech Products recalls Little Remedies New Baby Essentials Kit due to incorrect labeling of two items. Consumers should check kit lot numbers and contact the company for details.
Little RemediesMar 7, 2019 - Lower riskDrug
Boehringer Ingelheim Pharmaceuticals, Inc. recalls Mirapex (pramipexole dihydrochloride) Tablets, 1 mg, 100-count unit-dose tablets per folding carton, Rx only,
Boehringer Ingelheim recalls Mirapex 1mg tablets due to low weight detected in stability testing. Affected lots may have inconsistent dosing.
Boehringer IngelheimMar 7, 2019 - Lower riskDrug
Rising Pharmaceuticals, Inc. recalls Valsartan Tablets 40 mg USP, 30 tablet bottles, Rx, Only, Distributed by: Acetris Health, LLC, Saddle Brook, NJ,
Rising Pharmaceuticals recalls 40mg Valsartan tablets due to trace NDEA impurity found in some batches. Consumers should contact the manufacturer for details on affected lots.
Rising PharmaceuticalsMar 7, 2019 - Lower riskFood
GOOD KARMA FOODS INC recalls PL Trader Joe Natural Creamer - Vanilla 12/32oz, Plastic bottle, Distributed by Good Karma Foods, Inc. with
Good Karma Foods recalls PL Trader Joe Natural Creamer - Vanilla 12/32oz for undeclared milk. This product may contain milk without being listed on the label.
Good Karma FoodsMar 7, 2019 - Use cautionMedical device
PROCEPT BIOROBOTICS CORPORATION recalls AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301
Procept recalls specific lots of AquaBeam Handpiece (REF 310301, 320301) due to potential internal leaks from weld joint cracks. The device may become inoperable with error messages during use.
Procept BiometricsMar 6, 2019 - Lower riskMedical device
Topcon Medical Systems, Inc. recalls IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a software program that is intended for use in the collection,
Topcon recalls IMAGEnet 6 v1.53 software due to risk of displaying incorrect patient information on screen during use, potentially causing confusion in ophthalmic data systems.
TopconMar 6, 2019 - Lower riskMedical device
Acclarent, Inc. recalls TruDi NAV Suction, TDNS070Z, 70 Degree Tip Angle (01) 10705031245884
Acclarent recalls TruDi NAV Suction instruments with calibration issues that show incorrect tip orientation. Affected lots have a 30-cycle reprocessing shelf life.
AcclarentMar 6, 2019 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),
BioFire Diagnostics recalls GI Panel devices due to elevated false positives for Campylobacter and Cryptosporidium. Affected units have expiration dates from October 2019 onward. No remedy specified in recall notice.
BioFire DiagnosticsMar 6, 2019 - UnratedDrug
Preferred Pharmaceuticals, Inc recalls Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottle (NDC: 68788-0048-03), b) 90-count bottle (NDC:
Preferred Pharmaceuticals recalls Losartan Potassium Tablets (50mg) with NDC 68788-0048-03 and 68788-0048-09 due to presence of an impurity that may pose health risks. Affected products include 30-count and 90-count bottles.
Preferred PharmaceuticalsMar 6, 2019 - Stop using nowDrug
Dr. Reddy's Laboratories, Inc. recalls Docetaxel Injection USP, 80 mg/4 mL, (20 mg/mL), One-Vial Formulation, Rx only, Mfd By: Dr. Reddy's Laboratories
Dr. Reddy's recalls Docetaxel Injection due to defective container seals that may compromise sterility. Check lot H7081, exp 07/2019.
Dr. Reddy'sMar 6, 2019 - UnratedDrug
American Health Packaging recalls Valsartan Tablets USP 160 mg, 100 Tablets (10 x 10) per Unit Dose Blisters, Rx Only, Packaged and Distributed by:
American Health Packaging recalls Valsartan Tablets USP 160 mg due to detected NDEA, a carcinogen impurity in the active ingredient. Affected lots include Mar 2020 batch 179791.
American Health PackagingMar 6, 2019 - Use cautionVehicle
FORD E-450 (2018) recall — Exterior Lighting
Taylor Made Ambulances is recalling 2017-2018 Ford E-450 ambulances with Whelen brake lights that may illuminate without pressing the brake pedal. Owners should contact customer service for free replacement.
Taylor Made AmbulancesMar 5, 2019 - Use cautionMedical device
Fenwal Inc recalls Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and
Fenwal recalls CATSmart Continuous autotransfusion systems with specific model numbers and serial ranges due to risk of centrifuge tubing puncture during surgery.
FenwalMar 5, 2019 - Lower riskMedical device
Becton Dickinson & Company recalls Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
Becton Dickinson recalls Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07 due to kinked tubing in specific lots. Affected units may cause infusion issues.
Becton DickinsonMar 5, 2019 - UnratedDrug
AVKARE Inc. recalls Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only
AVKARE recalls 50-tablet unit dose boxes of losartan-hydrochlorothiazide tablets due to an impurity (NMBA) found during manufacturing. This could pose health risks to users.
AVKAREMar 5, 2019 - UnratedDrug
USA LESS Inc. recalls LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1
USA LESS Inc. recalls LEOPARD Miracle Honey (UPC 8 699415 910534) due to undeclared sildenafil. This unapproved drug poses safety risks as it lacks FDA approval for erectile dysfunction treatment.
USA LESSMar 5, 2019 - Stop using nowConsumer product
Arctic Cat Recalls Textron Off-Highway Utility Vehicles Due to Fuel Leak and Fire Hazard (Recall Alert)
Arctic Cat recalls 2019 Havoc off-highway utility vehicles with fuel leaks that could cause fire. Owners must stop using and contact Arctic Cat for free repair.
Arctic CatMar 5, 2019 - Stop using nowConsumer product
Arctic Cat Recalls Textron Off-Highway Utility Vehicles Due to Crash Hazard (Recall Alert)
Recall of 2018 Arctic Cat Stampede and Rust: Front suspension failure risks crashes. Stop using immediately and contact Arctic Cat for free repair.
Arctic CatMar 5, 2019 - Stop using nowVehicle
FORD TRANSIT (2017) recall — Equipment Adaptive/Mobility
Ricon recalls S-Series and K-Series wheelchair lifts for 2014-2017 Ford vans due to a positioning cam failure that can cause the platform to rise too high, risking user injury.
RiconMar 4, 2019
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