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- Lower riskFood
Euphoria Trading Company, LLC. recalls 70% Dark Chocolate Buttons packaged in cellophane bags, zip bags (plastic bag with Ziploc closure), a bulk bin in the
Euphoria Trading Company recalls 70% Dark Chocolate Buttons due to undeclared soy lecithin. Products sold with specific UPCs and lot codes from 2020.
Euphoria TradingJun 12, 2019 - Stop using nowConsumer product
Mares Recalls Buoyancy Compensation Vests Due to Drowning Hazard
Mares recalls XR buoyancy vests with serial numbers 8A-02001 to 8A-07630 due to deflation button unscrewing causing drowning. Consumers must stop using and get free repairs from authorized dealers.
MaresJun 12, 2019 - Stop using nowConsumer product
Hayward Industries Recalls Pool Heater Vent Kits Due to Carbon Monoxide Poisoning Hazard
Hayward recalls vent kits for H500FD gas pool heaters due to carbon monoxide leakage. Stop using the heater and contact Hayward for a free replacement.
HaywardJun 12, 2019 - Use cautionVehicle
BLUE BIRD VISION (2017) recall — Exterior Lighting
Blue Bird is recalling certain 2013-2020 Vision transit buses with Ford engines due to brake lights that may illuminate continuously, failing to warn following motorists when stopping.
Blue BirdJun 11, 2019 - Use cautionVehicle
BLUE BIRD VISION (2017) recall — Exterior Lighting
Blue Bird is recalling certain 2013-2020 Vision school buses with Ford engines due to brake lights potentially failing to warn following motorists of stopping. Owners must contact Blue Bird for a free repair.
Blue BirdJun 11, 2019 - Use cautionVehicle
FREIGHTLINER SPRINTER 4500 (2019) recall — Seats
Daimler Vans USA recalls 2019 Freightliner Sprinter 4500 vehicles with potential seat cushion shift in crashes. Owners must have front seat tilt adjusters replaced free by dealers.
Daimler Vans USAJun 11, 2019 - Lower riskMedical device
Randox Laboratories, Limited recalls Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use,
Randox recalls Human Assayed Multi-Sera Level 2 (HN1530) due to incorrect control values in specific lots. This may cause inaccurate diagnostic test results. Affected units include model HN1530 with serial numbers 1306UN, 1308UN, 1309UN.
RandoxJun 11, 2019 - UnratedMedical device
Life Technologies Corporation recalls StemPro¿ MSC SFM CTS"
Life Technologies recalls StemPro MSC SFM CTS devices with specific lot numbers due to untested supplier components. Affected units may have adventitious agents that could pose health risks.
Life TechnologiesJun 11, 2019 - Stop using nowConsumer product
Target Recalls Toddler Boots Due to Choking Hazard
Target recalls Cat & Jack Lilia toddler rain boots (sizes 5-12) due to unicorn horn detaching, posing choking hazard to young children. Consumers should stop using and return for refund.
Cat & JackJun 11, 2019 - Stop using nowConsumer product
Cushy Form Recalls Folding Mattress Due to Violation of Federal Mattress Flammability Standard; Sold Exclusively at Amazon.com (Recall Alert)
Cushy: Recalls white folding mattresses with lime green trim sold on Amazon for failing federal flammability standards. Consumers must stop using and get free fitted liner to prevent fire risk.
Cushy FormJun 11, 2019 - Stop using nowConsumer product
Amazon Recalls AmazonBasics Ceramic Space Heaters Due to Fire and Burn Hazards (Recall Alert)
Amazon recalls 1500W ceramic space heaters due to fire and burn risks. Affected models sold in black/silver with specific ASINs. Consumers must stop use and get refunds.
AmazonBasicsJun 11, 2019 - Lower riskMedical device
Santanello Surgical LLC recalls VAMPIRO V5001-minimally invasive poole suction sleeve that is an accessory instrument to ANY 5mm spot
Santanello Surgical recalls VAMPIRO V5001 minimally invasive poole suction sleeves due to potential sterility compromise from package integrity issues. Affected units have specific lot and UDI codes.
Santanel: SurgicalJun 10, 2019 - Use cautionMedical device
Olympus Corporation of the Americas recalls Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
Olympus recalls WM-NP2 and WM-DP2 mobile workstations with nurse control panel arms. If a video monitor weighs over 19.8 pounds, the workstation may become unstable and fall.
OlympusJun 10, 2019 - Lower riskMedical device
Molded Products Inc recalls Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Molded Products Inc recalls Luer Lock Set (Catalog # MPC-125) due to mislabeling in some packages. Affected units may be incorrectly labeled as MPC-150. No remedy specified in recall notice.
Molded ProductsJun 10, 2019 - Lower riskMedical device
Randox Laboratories, Limited recalls Assayed Bovine Multi-Sera Level 1, Model No. AL1027
Randox recalls Assayed Bovine Multi-Sera Level 1 Model AL1027 Lot 205SL due to potential bile acids measurement errors. Affected users should contact Randox for details.
RandoxJun 10, 2019 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Alinity ci -series System Control¿Module, Part Number 03R70 01 Product Usage: The Alinity ci series System Control
Abbott recalls Alinity ci series System Control Module (v2.6.0/v2.6.1) due to potential incorrect test results after system stops. Affected units may need software update to prevent errors.
AbbottJun 10, 2019 - UnratedMedical device
Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Zimmer Biomet recalls specific models of Comprehensive Reverse Shoulder Instrument Case (Outer Case Vault Only) due to inadequate sterilization validation. Affected units may not be properly sterilized, posing infection risks during surgical procedures.
Zimmer BiometJun 10, 2019 - Use cautionMedical device
Philips Medical Systems (Cleveland) Inc recalls BrightView XCT , Model Number 882482
Philips recalls BrightView XCT model 882482 handcontrollers that may move unexpectedly after button release, posing a risk of unintended motion during medical procedures.
Philips Medical SystemsJun 10, 2019 - UnratedDrug
Preferred Pharmaceuticals, Inc recalls Robafen DM, Generic for Robitussin DM, In each teaspoonful (5mL): Dextromethorphan HBr, USP 10mg,/Guaifenesin, USP
Preferred Pharmaceuticals recalls Robafen DM (generic for Robitussin DM) due to potential contamination with Burkholderia cepacia and Ralstonia pickettii. Affected lots were manufactured between February 2020 and July 2020. Consumers should contact the manufacturer for details.
Preferred PharmaceuticalsJun 10, 2019 - Stop using nowFood
Wismettac Asian Foods, INC recalls MONAKA BELGIUM CHOCO & KURUMI DAIICHI F, 2.68 oz. (76 g), Plastic wrapping Keep Frozen Product of Japan distributed by
Wismettac Asian Foods recalls frozen Monaka treats because they do not list coconut as an ingredient, posing a risk to those with allergies.
Wismettac Asian FoodsJun 10, 2019 - Lower riskFood
Tate & Lyle Ingredients Americas, LLC recalls Food starch, brand names Miraqk Mgl and Nustar 120 and Nustar 140
Tate & Lyle recalls food starch products Miraqk Mgl and Nustar 120/140 that may contain small wire pieces due to screen failure. Consumers should check lot numbers and contact the company for details.
Tate & LyleJun 10, 2019 - Use cautionMeat & poultry
Taylor Farms Illinois, Inc. Recalls Bacon Quiche Products due to Misbranding and Undeclared Allergens
USDA recalls 51 pounds of Taylor Farms bacon quiche products due to undeclared eggs, a known allergen. Consumers urged to stop using recalled items.
Taylor FarmsJun 9, 2019 - Use cautionVehicle
TEMSA TS45 (2016) recall — Equipment
Temsa is recalling 2013-2020 TS45 buses due to emergency exit labels that may not clearly show how to open windows quickly, potentially increasing injury risk during emergencies.
TemsaJun 9, 2019 - Use cautionVehicle
CHEVROLET TAHOE (2018) recall — Service Brakes, Hydraulic
Chevrolet is recalling 2018 Tahoe models with hydraulic brake assist issues that may increase stopping distance and crash risk. Owners must have their Electronic Brake Control Module reprogrammed free by dealers.
ChevroletJun 9, 2019 - Use cautionVehicle
CHEVROLET MALIBU (2018) recall — Electrical System
General Motors recalls 2018 Chevrolet Malibu vehicles with 1.5L turbo engines due to potential fuel injector failure causing engine stalling and crash risk. Owners will receive free software updates.
ChevroletJun 9, 2019 - Use cautionVehicle
BUICK ENCLAVE (2020) recall — Structure
General Motors recalls 2020 Buick Enclaves with possible frame rail cracks that could reduce crash performance. Owners should contact GM customer service for free inspection or replacement.
BuickJun 9, 2019 - Use cautionVehicle
BMW 128I (2012) recall — Electrical System
BMW recalls 2012 128i models with overheating wiring that could melt electrical connectors and cause fire. Owners must have blower-regulator wiring inspected and replaced free by dealers.
BMWJun 8, 2019 - Use cautionVehicle
TOYOTA RAV4 (2019) recall — Back Over Prevention
Toyota recalls 2019 RAV4s with backup camera that may not activate when reversing, increasing crash risk. Owners must have system inspected and repaired free by dealers.
ToyotaJun 8, 2019 - Use cautionMeat & poultry
Tyson Foods, Inc. Recalls Ready-To-Eat Chicken Fritter Products due to Possible Foreign Matter Contamination
Tyson Foods is recalling approximately 190,757 pounds of ready-to-eat chicken fritters that may contain hard plastic. Consumers should throw away or return products to the place of purchase.
Tyson FoodsJun 7, 2019 - Use cautionMedical device
Centurion Medical Products Corporation recalls Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Centurion recalls Sheridan Endotracheal Tubes in kit code TC7855 due to increased connector disconnection risk. Affected units may cause breathing issues during medical procedures.
CenturionJun 7, 2019
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83,517 recalls tracked · 71,995 explained in plain English · 10,969 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.