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
34,960 found- Use cautionConsumer product
Yamaha Recalls Golf Cars, Personal Transportation and Specialty Vehicles Due to Fire Hazard (Recall Alert)
Yamaha recalls 2017-2019 golf cars and specialty vehicles due to fire hazard from USB power module overheating. Owners must stop using USB charging devices and get free repairs.
YamahaAug 28, 2019 - Stop using nowConsumer product
Whirlpool Recalls Glass Cooktops with Touch Controls Due to Burn and Fire Hazards
Whirlpool recalls glass cooktops with touch controls from 2016-2019 due to risk of accidental activation causing burns and fires. Consumers must contact Whirlpool for free replacement.
WhirlpoolAug 28, 2019 - Stop using nowConsumer product
Kirkland's Recalls Chests of Drawers Due to Tip-Over and Entrapment Hazards
Kirkland's recalls two chest styles due to instability and entrapment risks for children. Stop using immediately to prevent tip-overs or injuries.
Kirkland'sAug 28, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Structure
Chrysler recalls 2019 RAM 1500 models with rear step kits that may cause fuel leaks during crashes, risking fire. Owners must have the step kit replaced free by dealers.
ChryslerAug 27, 2019 - Use cautionMedical device
Ad-Tech Medical Instrument Corporation recalls AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3-090-2.4N
Ad-Tech recalls drill sleeve guides (DSG-90-2.3N, DSG-6.3-090-2.4N) sold 2014-2019 due to potential drill bit seizing during surgery. Affected users should contact Ad-Tech for details.
Ad-TechAug 27, 2019 - Use cautionMedical device
NxStage Medical, Inc. recalls Low Volume Cartridge IFU (SKU CAR-125-B) used with the following devices: 1) NxStage One, Model NX1000-1; 2) NxStage
NxStage recalls low volume cartridges for home hemodialysis in patients with low blood volume (2.4L or less, under 30kg) to prevent health risks during dialysis treatments.
NxStageAug 27, 2019 - Lower riskMedical device
Karl Storz Endoscopy recalls Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope
Karl Storz recalls flexible pediatric neuroscopes with incorrect sterilization instructions that could lead to contamination if used with SS1E method. Affected models include 11282BN1.
Karl StorzAug 27, 2019 - Lower riskDrug
American Health Packaging recalls Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC:
American Health Packaging recalls Lamivudine 150mg tablets with incorrect labeling that may cause dosage confusion. Affected lots expire June 2021. Consumers should check NDC 60687-362-21.
American Health PackagingAug 27, 2019 - Lower riskFood
BAKKAVOR USA recalls Savory Tuna salad 16 oz. packaged in Clear PP containers UPC 4122033749
BAKKAVOR USA recalls 16 oz. Savory Tuna salad with undeclared shrimp. Consumers should check UPC 4122033749 and avoid consumption due to potential allergic reactions.
BAKKAVOR USAAug 27, 2019 - Stop using nowConsumer product
Happy Plugs Recalls Wireless Headphones Due to Burn Hazard
Happy Plugs Wireless II Bluetooth Headphones with micro-USB charging cable may overheat, causing burns. Recalled units include specific colors and UPCs; return for free replacement.
Happy PlugsAug 27, 2019 - Stop using nowConsumer product
Contigo Recalls 5.7 Million Kids Water Bottles Due to Choking Hazard
Contigo recalls 5.7M kids water bottles because the silicone spout can detach, posing a choking hazard. Stop use and contact Contigo for a free replacement lid.
ContigoAug 27, 2019 - Stop using nowConsumer product
At Home Recalls Shag Rugs Due to Violation of Federal Flammability Standard; Fire Hazard
At Home's large shag rugs fail federal flammability standards, posing fire risk. Small rugs lack required flammable labels. Consumers must stop using and get refunds or labels.
At HomeAug 27, 2019 - Use cautionVehicle
LANCE CAMPER LANCE CAMPER (2019) recall — Electrical System
Lance Camper is recalling 2018-2019 855S trailers due to potential refrigerator wiring shorting out and causing fire. Owners must have a clamp installed by dealers.
Lance CamperAug 26, 2019 - Use cautionVehicle
AUTOCAR XPEDITOR (2019) recall — Steering
Autocar is recalling 2019-2020 Xpeditor vehicles with potentially loose power steering mounting bolts that could cause loss of vehicle control. Owners should contact Autocar customer service for free repairs.
AutocarAug 26, 2019 - Use cautionVehicle
BRAXTON CREEK BUSHWACKER (2020) recall — Equipment
Braxton Creek is recalling 2020 Bushwhacker trailers that may lack LP/CO detectors, risking carbon monoxide poisoning. Owners must contact customer service for free detector installation.
Braxton CreekAug 26, 2019 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls Positron Emission Tomograpy and Computed Tomography System, Model: uMI 550, with software version R001.3.0.0.750505, Rx
Shanghai United Imaging Healthcare recalls uMI 550 PET/CT scanners with specific software version R001.3.0.0.750505 due to potential PET acquisition data issues that could lead to rescans and additional patient radiation doses. Affected units have serial numbers 200017 and 200023.
Shanghai United Imaging HealthcareAug 26, 2019 - Stop using nowMedical device
LivaNova Deutschland GmbH recalls Control Panel REF - 60-02-15: LivaNova SCP Pump Control Panel. REF 60-02-15, IPX2, RxOnly, UDI: 04033817900986
LivaNova recalls SCP Pump Control Panel REF 60-02-15 due to potential angle encoder failure causing stroke, organ damage, or arterial injury during heart surgery. Affected units have specific serial numbers and UDI codes.
LivaNovaAug 26, 2019 - Lower riskDrug
EPI Health, LLC recalls minolira (minocycline hydrochloride) extended-release tablets 135 mg* Physician Sample Not for Sale 5 Tablets, Rx Only,
EPI Health recalls 135mg minol: Extended-release tablets may not dissolve properly, risking ineffective treatment. Check NDC 71403-102-05, lot T900093, exp 11/2020.
EPI HealthAug 26, 2019 - Use cautionFood
Suntree Snack Foods, LLC recalls Nice! Espresso Trail Mix, Net Wt 2.5 Oz (70g) Pouch. Distributed by Sun Tree Snack Foods, LLC, Ambient Storage
Suntree Snack Foods recalls Nice! Espresso Trail Mix due to undeclared sulfites. Check lot numbers and code dates for affected pouches.
Nice!Aug 26, 2019 - Lower riskFood
Natures One Inc recalls PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can
Natures One recalls PediaSmart Organic Soy Vanilla Beverage Mix due to undeclared milk allergen. Affected lots have specific use-by dates; consumers should check labels and contact company for details.
Natures OneAug 26, 2019 - Lower riskFood
Hometown Food Company recalls Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case.
Hometown Food Company recalls 12-pouch cases of Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix due to gluten contamination despite being labeled gluten-free. Products with lot codes 9204 or 9205 and best by dates January 23-24, 2021 are affected.
Hometown Food CompanyAug 26, 2019 - Lower riskFood
Valencia Flour Mill, Ltd. recalls Valencia Sopaipilla and Fry Bread Mix, 25 lbs, packaged in Paper bags with polyliners. UPC 7 30701 22025 3
Valencia Flour Mill recalls 25-lb sopaipilla and fry bread mixes containing undeclared milk. Consumers should check UPC 7 30701 22025 3 for affected products.
Valencia Flour MillAug 26, 2019 - Stop using nowConsumer product
BRP Recalls Snowmobiles Due to Fire Hazard (Recall Alert)
BRP recalls 2019 Ski-Doo snowmobiles with 850 E-TEC engines due to potential fuel leaks causing fire. Affected models include Backcountry, Freeride, MXZ, Renegade, and Summit series. Consumers must stop using and contact BRP for free repairs.
BRPAug 26, 2019 - Stop using nowMeat & poultry
Olympia Meats Recalls Ready-To-Eat Pork Sausage Products due to Misbranding and Undeclared Allergens
Olympia Meats recalls ~198 lbs of ready-to-eat pork sausage because it contains undeclared pistachios. Do not consume; discard or return.
Olympia ProvisionsAug 24, 2019 - UnratedDrug
Tuscano and Delucia Group (DBA Entropic Labs) recalls Entropic Labs SARM RAD-140, 20mg Capsules, 30-count bottles, Entropic Labs UPC#: 651074545302
Entropic Labs recalls 20mg RAD-140 capsules due to being marketed without FDA approval. This unapproved SARM product may pose health risks. Consumers should check their bottles for the UPC 651074545302.
Entropic LabsAug 24, 2019 - UnratedMedical device
Elekta, Inc. recalls Monaco Radiation Treatment Planning System (RTP) System
Elekta recalls Monaco radiation treatment software versions 5.50.00 and 5.51.00 due to incorrect anatomy and beam shift display in reports, which could lead to improper radiation targeting.
Elek: The brand name from the manufacturer title isAug 23, 2019 - Use cautionMedical device
Ra Medical Systems, Inc. recalls Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 Excimer Laser System is designed to treat the
Ra Medical Systems recalls EX-30:8 excimer laser systems due to software error causing over-treatment risks. Affected units may cause skin blisters or strong redness. Contact for remedy.
Ra Medical SystemsAug 23, 2019 - Lower riskMedical device
Philips North America, LLC recalls IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined
Philips recalls IntelliVue 1.4 GHz Remote Antennas used with MX40 monitors that have inadequate cable ratings for certain installations. Affected units shipped since May 2019 with 'CM' marked coax data cable. Serial numbers listed in the recall.
PhilipsAug 23, 2019 - UnratedDrug
Aurolife Pharma, LLC recalls Fexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 62011-0315-1); and b) 30-count
Aurolife Pharma recalls 180mg fexofenadine tablets with specific lot numbers due to failed impurities and degradation specifications. Consumers should check their packaging for NDC codes and lot numbers to determine if affected.
AurolifeAug 23, 2019 - Lower riskFood
Krasnyi Oktyabr Inc. USA recalls TAINY VOSTOKA ASSORTED DRIED FRUITS - QUINCE packaged in 500gram (17.65oz), clear plastic package marked with container
Krasnyi Oktyabr USA recalls dried quince products with undeclared sulfites. Affected items have specific lot codes and expiration dates. Consumers should check packaging for recall details.
Krasnyi OktyabrAug 23, 2019
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