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
34,893 found- Stop using nowConsumer product
Dr. Martens Vegan Boots Recalled by Airwair Due to Chemical Exposure Hazard
Dr. Martens vegan 1460 boots sold in cherry red with black laces recalled due to benzidine exposure risk from tongue lining. Consumers must stop using and get refund or replacement.
Dr. MartensAug 24, 2017 - Stop using nowConsumer product
Arc'teryx Recalls Ski Mountaineering Boots Due to Fall Hazard
Arc'teryx recalls Procline ski mountaineering boots with a fall hazard due to dislodging axis pins. Affected models include men's and women's sizes 7½ to 10½. Return to dealer for free repair.
Arc'teryxAug 24, 2017 - Use cautionMeat & poultry
Expresco Foods Inc. Recalls Chicken Skewer Products Due to Possible Listeria Contamination
USDA FSIS recalls Expresco chicken skewers from 2017 with possible Listeria monocytogenes contamination. Consumers urged to discard products with specific UPC codes and lot numbers.
Expresco FoodsAug 23, 2017 - Use cautionVehicle
GILLIG LOW FLOOR (2016) recall — Seat Belts
Gillig is recalling certain 2017-2018 Low Floor transit buses with Recaro seats due to seat belt buckles that may get stuck, preventing safe use in crashes.
GilligAug 23, 2017 - Use cautionVehicle
TOYOTA HIGHLANDER (2017) recall — Equipment
Gulf States Toyota recalls 2017 Highlander vehicles with roof rail cross bars that may loosen and detach, increasing crash risk. Owners must have dealers inspect fasteners for free.
Gulf States ToyotaAug 23, 2017 - Use cautionVehicle
FOREST RIVER FLAGSTAFF (2018) recall — Suspension
Forest River recalls 2018 Flagstaff trailers with Dexter axles due to potential hub bearing failure causing loss of vehicle control. Owners should contact customer service for free replacement of affected parts.
Forest RiverAug 23, 2017 - Lower riskMedical device
North Star Imaging Inc recalls North Star Imaging Inc. (NSI) Model X-7000 industrial cabinet x-ray system. Industrial x-ray imaging of product hardware
North Star Imaging recalls X-7000 industrial x-ray systems due to low-level radiation leaks. Affected units may pose radiation exposure risks during industrial imaging operations.
North Star ImagingAug 23, 2017 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Human Alpha-1-Antitrypsin Kit for use on the SPAPlus analyser, Product #NK034.S. The firm name on the label is The
The Binding Site recalls Human Alpha-1-Antitrypsin Kit for SPAPlus analyser due to potential low control values affecting test accuracy. This may impact liver and lung condition diagnosis.
The Binding SiteAug 23, 2017 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Syngo.plaza systems with SW VB20A, Model Number - 10863171, 10863172, 10863173 Product Usage: Syngo.plaza is a Picture
Siemens recalls Syngo.plaza PACS systems with specific model numbers due to workflow display errors when replacing studies. Affected units may show outdated studies in some workflow steps.
SiemensAug 23, 2017 - Use cautionMedical device
Philips Electronics North America Corporation recalls IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2,
Philips recalls IntelliVue Multi Measurement Servers with 12-lead ECG monitoring that may show distorted ST-segments, potentially affecting patient diagnosis. Affected models include M300IA/AL, M3002A, M8102A, M8105A with specific firmware and 12-lead options.
PhilipsAug 23, 2017 - Lower riskDrug
Inopak Ltd recalls Option Systems Antibacterial Foaming Hand Wash, 0.3% P.C.M.X., 8 fl oz and 18 fl oz. bottles and 500, mL 800 mL, and
Inopak recalls antibacterial hand wash products due to potential bacterial contamination from a contaminated diaphragm pump. Affected items include 8 fl oz and 18 fl oz bottles and pouches with specific batch numbers.
InopakAug 23, 2017 - Stop using nowConsumer product
Nutrilife Recalls Bottles of Hydrogen Peroxide Due to Fire, Burn Hazards
Nutrilife recalls 29% hydrogen peroxide one-gallon bottles due to bottle caps that can cause pressure buildup, leading to fire and burn risks. Consumers should stop using and get free replacement caps or refunds.
NutrilifeAug 23, 2017 - Stop using nowConsumer product
Academy Sports + Outdoors Recalls Crawfish Kits with Strainer Due to Fire Hazard
Academy Sports recalls 100-quart crawfish kits with strainer due to fire hazard from melting hose. Consumers must stop using and get free replacement hose assembly.
Academy Sports + OutdoorsAug 23, 2017 - Use cautionMeat & poultry
Fair Oaks Farms, LLC Recalls Pork Sausage Patties Due to Possible Listeria Contamination
Fair Oaks Farms recalls pork sausage patties from August 2017 due to possible Listeria monocytogenes contamination. Consumers are urged not to consume these products.
Fair Oaks FarmsAug 22, 2017 - Use cautionVehicle
CHEVROLET EQUINOX (2018) recall — Power Train
Chevrolet is recalling 2018 Equinox vehicles with a risk of losing propulsion if the front right drive shaft separates, potentially causing crashes. Owners must have the drive shaft replaced free of charge.
ChevroletAug 22, 2017 - Lower riskMedical device
Siemens Medical Solutions USA, INC recalls Artis oneFloor-mounted system for uncompromised imaging; Artis one, Interventional fluoroscopic x-ray system, Artis one
Siemens recalls Artis one systems with specific serial numbers for potential display issues that could affect imaging quality. Affected units may show blinking or blue/black screens during use.
SiemensAug 22, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Ziptight Ankle Syndesmosis Fixation Device, Titanium Implant Titanium Implant for surgical repairs of soft tissue.
Zimmer Biomet recalls Ziptight Ankle Syndesmosis Fixation Devices due to missing tip protectors in packaging. This could lead to improper use during surgical repairs.
Zimmer BiometAug 22, 2017 - Use cautionMedical device
Smiths Medical ASD Inc. recalls Medfusion, Syringe Infusion Pump, Software Version V1.1, Rx Only, Manufactured by Smiths Medical ASD, Inc., 1500 Eureka
Smiths Medical recalls Medfusion syringe infusion pumps with software version V1.1 due to potential syringe size detection errors. Affected units may trigger "Invalid Syringe Size" alarms during fluid administration. Contact for remedy details.
Smiths MedicalAug 22, 2017 - Stop using nowDrug
Pfizer Inc. recalls HYDROmorphone HCl Injection, USP, 2 mg/mL, 1mL Single-use vial, packaged in cartons of 25 vials, Rx only, Hospira,
Pfizer recalls specific lots of Hydromorphone HCl Injection due to lack of sterility assurance. Check your vials for lot number 760853A.
Pfizer / HospiraAug 22, 2017 - Use cautionDrug
RemedyRepack Inc. recalls Ketorolac Trom 30 mg/mL Injection, packaged in a) 1 mL vials, NDC 61786-0741-01 (Orig: 00548-9021-00), Ref: 33631 and
RemedyRepack recalls Ketorolac 30 mg/mL injections with visible crystalline particles that could cause serious injury if injected.
RemedyRepackAug 22, 2017 - UnratedDrug
Wockhardt Usa Inc. recalls Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C.
Wockhardt recalls 5mg enalapril tablets due to impurities. Affected products have specific NDC and lot numbers. Stop using if you have these items.
WockhardtAug 22, 2017 - UnratedDrug
Centurion Labs, LLC recalls Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz.
Centurion Labs recalls Ninjacof-A oral solution due to potential B. cepacia contamination. Consumers should check product details and contact the company for guidance.
Centurion LabsAug 22, 2017 - UnratedDrug
Shata Trading, Inc. recalls No. 1 Faiza Beauty Cream Manufactured by: Poonia Brothers (Pak), Gujranwala, Distributed by Shata Traders Inc., 4, 19th
Shata Trading recalls No. 1 Faiza Beauty Cream manufactured by Poonia Brothers (Pak) due to being marketed without FDA approval. This product may not be safe for use. Consumers should check the UPC and batch number for affected items.
Shata TradingAug 22, 2017 - Lower riskDrug
Sage Products Inc recalls Toothette Oral Care Suction Toothbrushes with Perox-A-Mint solution. Contains 2 Suction Toothbrushes with sodium
Sage Products recalls Toothette Oral Care Suction Toothbrushes with Perox-A-Mint solution due to cross contamination with non-pharmaceutical products during manufacturing. Affected units include specific product codes and expiration dates.
Sage ProductsAug 22, 2017 - Use cautionFood
Joy's International Foods recalls Joy's Gourmet Olive Tapenade, All Natural, Net Wt. 10 OZ. (280g).
Joy's International Foods recalls Gourmet Olive Tapenade due to unrecorded temperatures after thermal processes. Check your best-by dates for affected lots.
Joy's International FoodsAug 22, 2017 - Stop using nowConsumer product
Polaris Recalls GENERAL Recreational Off-Highway Vehicles Due to Crash Hazard (Recall Alert)
Polaris recalls 2017 General Base and Hunter off-highway vehicles due to inconsistent tire pressure labels risking crashes. Owners must stop using and contact for updated manual.
PolarisAug 22, 2017 - Use cautionVehicle
BMW R1200 GS (2017) recall — Exterior Lighting
BMW recalls certain 2017 R1200 GS models with insufficiently visible turn signals, risking crashes. Owners must have turn signals replaced free by dealers.
BMWAug 21, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer is intended for use as an in vitro diagnostic device for
Beckman Coulter recalls AQUIOS CL Flow Cytometers with specific serial numbers due to software settings causing incorrect patient test results. Affected units may report wrong lab values for some samples.
Beckman CoulterAug 21, 2017 - Stop using nowFood
SUNOPTA GRAINS AND FOODS recalls Organic Great Value Dark Sweet Cherry Products Pitted, Net Wt 32 Oz (2 lb) 907 g, Distributed by Wal-Mart Stores, Inc.
Sunopta recalls organic dark sweet cherry products due to Listeria monocytogenes found in a sample. Consumers should check labels for best by date 08/10/19.
SunoptaAug 21, 2017 - Use cautionVehicle
HEARTLAND PIONEER (2018) recall — Equipment
Heartland is recalling 2018 Pioneer trailers (RD210, BH270, BH250) due to propane hose not securely attached, risking leaks and fires. Owners must contact Heartland for free hose clamp installation.
HeartlandAug 18, 2017
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