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
34,943 found- Use cautionVehicle
THOR MOTOR COACH OUTLAW (2019) recall — Electrical System
Thor Motor Coach is recalling certain 2018-2019 Outlaw motorhomes due to a potential electrical short that could cause fire. Owners should contact TMC for free wiring repairs.
Thor Motor CoachAug 29, 2018 - Lower riskMedical device
Incisive Surgical Inc recalls INSORB SUBCUTICULAR SKIN STAPLER, REF 2030
Incisive Surgical recalls Insorb Subcutaneous Skin Stapper model REF 2030 due to possible sterile barrier compromise. Affected units include specific lot numbers and UDI codes.
Incisive SurgicalAug 29, 2018 - Lower riskMedical device
Data Innovations, LLC recalls IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software product that can receive information from a
Data Innovations recalls IM Abbott Alinity ci-series software v8.00.0001 that may cause quality control results to not process, potentially delaying or misdirecting patient treatment. No patient harm has been reported.
Data InnovationsAug 29, 2018 - Use cautionMedical device
SANRAI INTERNATIONAL LLC recalls Sunset Compressor Nebulizer, Model NEB100 - Product Usage: The Sunset Compressor Nebulizer is an AC-powered air
SANRAI recalls Sunset Compressor Nebulizer Model NEB100 for potential overheating when used in 220V countries like South Africa, where it's designed for 120V systems.
SANRAIAug 29, 2018 - Lower riskFood
CAMPOMEX USA CORP recalls Campomex USA fresh cilantro: 5 dozens (60) per box.
Campomex USA recalls fresh cilantro due to Cyclospora contamination from a pallet mistakenly distributed. Consumers should avoid affected products to prevent foodborne illness.
Campomex USAAug 29, 2018 - Stop using nowFood
Cedarlane Natural Foods Inc/Frankly Fresh Foods Inc. recalls CedarLane Organic Salads; Couscous, Veggies & Chickpeas with Citrus Dressing. NET WT 9 oz. -Gluten Free -Vegetarian
Cedarlane recalls gluten-free salads and couscous products that contain undetected wheat, posing a risk for people with celiac disease or gluten allergies. Products were sold from 9/05/2018 to 10/19/2018.
CedarlaneAug 29, 2018 - Stop using nowConsumer product
Cybex Recalls Weight-Lifting Equipment Due to Serious Injury Hazards
Cybex recalls Smith Press models 5340 and 5341 (1989-2009) due to weight bar falling risk. Consumers must stop using immediately and get free repairs or refunds.
CybexAug 29, 2018 - Use cautionConsumer product
BSN SPORTS Recalls Rubber Critter Toys Due to Violation of Federal Lead Paint Ban (Recall Alert)
BSN SPORTS recalls rubber critter toys with lead paint exceeding federal limits. Lead can harm children's health if ingested. Consumers should stop using and contact for credit.
BSN SPORTSAug 29, 2018 - Use cautionVehicle
MAC TRAILERS WASTE TRAILER (2019) recall — Wheels
MAC is recalling 2019 Dump and Waste Trailers due to potential wheel end separation from axle, increasing crash risk. Owners should contact MAC for free inspection.
MACAug 28, 2018 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Equipment
Blue Bird is recalling 2019 All American and 2019-2020 Vision school buses with NextGen seats that may lack a warning label, risking improper child restraint use. Owners must get a free label fix from dealers.
Blue BirdAug 28, 2018 - Lower riskMedical device
Heartware, Inc. recalls Heart Ware(TM) HVAD(TM) System Controller/Controller Kits, Model Numbers: 1403, 1407, and 1420 Product Usage: The
Heartware recalls HVAD System Controllers (models 1403, 1407, 1420) due to potential hairline cracks at power ports from water/fluid exposure. Affected units have serial numbers CON300175 to CON320540.
HeartwareAug 28, 2018 - Use cautionMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo 220/240V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass procedures. Catalog
Terumo recalls specific models of Advanced Perfusion System Platform for cardiopulmonary bypass use due to potential electrical short from improperly torqued screws. Affected units may need repair or replacement.
TerumoAug 28, 2018 - Lower riskMedical device
Abbott Laboratories, Inc recalls Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip
Abbott recalls ARCHITECT cSystems ICT Module REF 09D28-03 for potential false elevated chloride test results. Affected units may give inaccurate blood chloride readings.
AbbottAug 28, 2018 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only
Ortho-Clinical Diagnostics recalls VITROS Vitamin B1:2 Reagent Packs (Catalog 1453489) due to potential calibration failures affecting vitamin B12 test accuracy. Affected lots 2601, 2610, 2620.
Ortho-Clinical DiagnosticsAug 28, 2018 - Lower riskMedical device
Alcon Research, LTD. recalls CyPass System 241-S, CYPASS MICRO-STENT, CYPASS LOADED, CYPASS APPLIER, REF CATALOG #: 8065754003 For ophthalmic use.
Alcon recalls CyPass Micro-Stent devices due to statistically significant endothelial cell loss in long-term studies. Affected units include specific model numbers and lot/serial numbers. No immediate action required per recall details.
AlconAug 28, 2018 - Lower riskMedical device
Hitachi Healthcare Americas Corp Informatics Division recalls VidiStar(TM) PACS & DICOM Viewer Software system
Hitachi Healthcare recalls VidiStar PACS & DICOM Viewer Software versions 3.10.5 and : intermixed patient images in studies could cause misdiagnosis.
Hitachi HealthcareAug 28, 2018 - Use cautionMedical device
Stryker GmbH recalls Hoffman LRF Hexapod Strut, Extra Short 183mm-295mm, Model Number 4935-0-040. Product Usage - The Hoffmann LRF System is
Stryker recalls Hoffman LRF Hexapod Struts with model 4935-0-040 due to potential pin displacement causing instability. Affected units sold in specific lots; contact Stryker for remedy.
StrykerAug 28, 2018 - UnratedDrug
Pfizer Inc. recalls Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 2.5 mL Single-use Vial, Rx only, Sterile, Manufactured for: Hospira,
Pfizer recalls Argatroban injection vials due to impurities and stability issues. Patients with blood clotting conditions should contact their doctor immediately.
PfizerAug 28, 2018 - Lower riskDrug
Humco Holding Group, Inc recalls Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only
Humco recalls thyroid medication with inconsistent levothyroxine and liothyronine levels. This may cause incorrect dosing. Contact Humco for details.
HumcoAug 28, 2018 - Use cautionVehicle
JAYCO REDHAWK (2017) recall — Visibility
Jayco is recalling 2015-2017 Redhawk motorhomes with driver side window switches prone to corrosion causing fire risk. Owners must have the switch replaced free by GM dealers.
JaycoAug 27, 2018 - Lower riskMedical device
Arthrex, Inc. recalls Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the
Arthrex recalls Li-ion battery housings for AR-400 DrillSaw Sports 400 systems due to potential fluid ingress. Affected units have specific batch numbers and material codes.
ArthrexAug 27, 2018 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls MethylPREDNISolone Tablets, USP, 4 mg, 21-count blister pack. Rx Only. Jubilant Cadista Pharmaceuticals Inc. Salisbury,
Jubilant Cadista recalls 4mg MethylPREDNISolone tablets due to stability testing failure. Rx-only medication with specific lot numbers and expiration date.
Jubilant CadistaAug 27, 2018 - Lower riskDrug
QuVa Pharma, Inc. recalls Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx only, QuVa Pharma, 519 Route 173,
QuVa Pharma recalls Norepinephrine 4 mg bags due to potential lack of active ingredient. Affected units may not deliver proper medication dose.
QuVa PharmaAug 27, 2018 - Lower riskDrug
SCA Pharmaceuticals, Inc. recalls Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA
SCA Pharmaceuticals recalls Furosemide 100 mg injection with visible precipitate. This may affect drug effectiveness. Check product lot numbers for affected batches.
SCAAug 27, 2018 - Lower riskDrug
Mylan Pharmaceuticals Inc. recalls Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg/0.03 mg, Rx Only, 3 extended-cycle blister packs containing
Mylan Pharmaceuticals recalls 3 extended-cycle birth control pill packs with incorrect labeling on blister packs. This affects prescription-only pills sold in India with specific NDC and lot numbers.
MylanAug 27, 2018 - Stop using nowConsumer product
Polaris Recalls RZR XP Turbo S Recreational Off-Highway Vehicles Due to Injury Hazard (Recall Alert)
Polaris recalls 2018 RZR XP Turbo S off-highway vehicles due to rollover protection structure failure in high-speed rollovers. Owners must stop using and contact a dealer for free repair.
PolarisAug 27, 2018 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Empire Kosher Poultry, Inc. Raw Chicken Products due to Possible Salmonella Contamination
U.S. Department of Agriculture's Food Safety and Inspection Service recalls Empire Kosher raw chicken products due to possible Salmonella contamination linked to illnesses in the Northeast and Mid-Atlantic U.S.
Empire KosherAug 24, 2018 - Use cautionVehicle
IC BUS CESB (2016) recall — Equipment Adaptive/Mobility
Navistar recalls 2015-2019 IC Bus school buses with certain wheelchair lifts that may tip users toward the vehicle when exiting, increasing injury risk. Owners must replace faulty cams free of charge.
NavistarAug 24, 2018 - Use cautionMedical device
Inpeco S.A. recalls FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) (same product) FlexLab, Accelerator a3600 and Aptio
Inpeco recalls FlexLab, Accelerator a3600 and Aptio Automation modular systems due to missing safety pacemaker labels. People with pacemakers must maintain 200mm distance from modules to avoid malfunction.
InpecoAug 24, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls Beckman Coulter Lipase, REF OSR6130 and OSR6230.
Beckman Coulter recalls Lipase test kits OSR6130 and OSR6230 due to potential NAPQI interference in overdose patients. All lots affected.
Beckman CoulterAug 24, 2018
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