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 cautionMedical device
Zimmer Biomet, Inc. recalls Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1030-12 Used for the
Zimmer Biomet recalls 12-pack of 16MM RapidFlap SpinDown Clamps due to incorrect assembly, which may cause injury during surgery. Affected units have lot expiry before 09/18/2023.
Zimmer BiometAug 22, 2018 - Lower riskDrug
Syntec Pharma Corp recalls THYROID POWDER USP (Levothyroxine labeled range of 34.2-41.8mcg/grain; Liothyroine (correct spelling Liothyronine):
Syntec Pharma recalls thyroid powder USP due to inconsistent levothyroxine and liothyronine levels. This may affect medication dosing accuracy for patients using prescription thyroid hormone.
Syntec Pharma CorpAug 22, 2018 - Stop using nowConsumer product
Yamaha Recalls Snowmobiles Due to Injury Hazard (Recall Alert)
Yamaha recalls 2018 SRVenture DX snowmobiles with loose handgrips that could cause falls and severe injury. Owners must stop using and get free repairs.
YamahaAug 22, 2018 - Stop using nowConsumer product
Vornado Air Reannounces Recall of Electric Space Heaters Following Report of Death; Fire and Burn Hazards
Vornado VH101 Personal Vortex electric space heaters recalled due to fire and burn risks from overheating. Consumers must stop using and contact Vornado for refund or replacement.
VornadoAug 22, 2018 - Use cautionMeat & poultry
Taylor Farms Northwest, LLC Recalls Ready-To-Eat Meatloaf Products Due To Misbranding and Undeclared Allergens
USDA recalls Taylor Farms Northwest LLC's ready-to-eat meatloaf products for misbranding and undeclared allergens like fish and milk. Consumers are urged not to consume these products.
Taylor FarmsAug 21, 2018 - Use cautionVehicle
FOREST RIVER SALEM (2019) recall — Electrical System
Forest River is recalling 2014-2019 Salem trailers due to potential brake failure if trailer detaches from tow vehicle, requiring free wiring harness fix.
Forest RiverAug 21, 2018 - UnratedMedical device
OriGen Biomedical, Inc. recalls Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF:
OriGen Biomedical recalls reinforced dual lumen cannulas due to failed endotoxin testing. Affected units have specific model and lot numbers. Consumers should contact for details.
OriGen BiomedicalAug 21, 2018 - Lower riskMedical device
Exactech, Inc. recalls Equinoxe Reverse Drill Bit Kit, Catalog Number 321-20-00 Product Usage: Shoulder surgery
Exactech recalls Equinoxe Reverse Drill Bit Kit (Catalog 321-20-00) for shoulder surgery due to incorrect drill bit configuration. Affected units have serial numbers 5214432 and 5214445.
ExactechAug 21, 2018 - UnratedMedical device
Coltene Whaledent Inc recalls ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into
Coltene Whaledent recalls ParaPost Plus 25 Titanium Alloy Dental Posts (Catalog P2845B) due to stainless steel components potentially causing injury during dental procedures.
Coltene WhaledentAug 21, 2018 - Lower riskMedical device
Genicon, Inc. recalls Genicon GENILook Model 200-005-152, 5mm diameter, 100mm legnth (2 cannula, threaded) - Product Usage: The universal
Genicon recalls its GENILook Model 200-005-152 surgical device due to potential plastic tip detachment from metal shaft. Affected units sold with lot number I7717-C.
GeniconAug 21, 2018 - Lower riskMedical device
OriGen Biomedical, Inc. recalls Reinforced Dual Lumen Cannula, 32Fr., REF: VV32F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is
OriGen recalls 32Fr Reinforced Dual Lumen Cannulas (REF: VV3: VV32F) due to potential barium sulfate omission and incorrect tip length. This affects medical use in extracorporeal life support.
OriGenAug 21, 2018 - Lower riskDrug
Sichuan Friendly Pharmaceutical Co.,Ltd. recalls Thyroid Powder 25kg/drum, US Pharmacopoeia, Sichuan Friendly Pharmaceutical Co., LTD, Production Address: No. 680,
Sichuan Friendly Pharmaceutical recalls Thyroid Powder 25kg/drum (NDC 7807-0170-11) due to inconsistent levothyroxine and liothyronine levels. Affected lots include 160601-170702. Consumers should check their lot numbers and contact the manufacturer.
Sichuan Friendly PharmaceuticalAug 21, 2018 - UnratedDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 100 mL bags, Rx only, Baxter Healthcare Corporation Deerfield, IL 60015 USA, NDC
Baxter Healthcare recalls 0.9% Sodium Chloride Injection USP 100 mL bags (Rx only) due to CGMP deviations. Affected lots include P380287 expiring 12/2019. No specific remedy is stated in the recall notice.
Baxter HealthcareAug 21, 2018 - Lower riskDrug
Accord Healthcare, Inc. recalls Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham,
Accord Healthcare recalls 100-count Hydrochlorothiazide tablets after customer complaints of containing Spironolactone instead. This mix-up could lead to incorrect medication use. Check your prescription bottle for the label and contact your pharmacy.
Accord HealthcareAug 21, 2018 - Lower riskDrug
Mayne Pharma Inc recalls Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma,
Mayne Pharma recalls 100-count oxycodone and acetaminophen tablets due to mislabeled lot numbers on packaging, which could lead to confusion in tracking expiration dates.
Mayne PharmaAug 21, 2018 - Lower riskDrug
Auro Pharmacies, Inc. recalls Methyl-Cobalamin injectable, 1 mg/mL, packaged in a) 5 mL and b) 30 mL Multiple Dose vials, Rx only, Central Drugs
Auro Pharmacies recalls methyl-cobalamin injectables (5mL and 30mL vials) due to lack of sterility assurance. Products may cause infection if used improperly.
Auro PharmaciesAug 21, 2018 - UnratedFood
Lipari Foods Operating Company, LLC dba JLM Manufacturing recalls Premo Brand Turkey & Cheese Wedge sandwiches 5 OZ retail UPC 612510002018 Plastic triangle sandwich wedge container
Premo Turkey & Cheese Wedge sandwiches (5 oz) with UPC 612510002018 recalled due to potential Listeria monocytogenes contamination. Consumers should check labels and contact Lipari Foods for details.
PremoAug 21, 2018 - Stop using nowConsumer product
Confer Plastics Recalls Pool Step Systems Due to Entrapment and Drowning Hazard
Confer Plastics recalls three pool step models from 2013-2018 due to children's limbs getting trapped in side openings, risking drowning. Consumers must stop using and get a free repair kit.
Confer PlasticsAug 21, 2018 - Use cautionVehicle
VOLKSWAGEN ATLAS (2018) recall — Air Bags
Volkswagen recalls 2018 Atlas vehicles with twisted air conditioning drain tubes that may cause air bags to deploy unintentionally, increasing injury risk. Owners must have air bag control modules replaced at dealers.
VolkswagenAug 20, 2018 - Use cautionVehicle
FORD FLEX (2019) recall — Electrical System
Ford recalls 2019 Flex vehicles with unsecured alternator and starter cables that may cause electrical arcs and fire risk. Owners must have cables checked by dealers free of charge.
FordAug 20, 2018 - Lower riskMedical device
ICU Medical, Inc. recalls ICU Medical 14" (36 cm) Appx 3.6 ml, Bifuse Transfer Set w/Rotating Luer, REF: 14237-28 The Intravascular
ICU Medical recalls 14" Bifuse Transfer Sets (REF: 14237-28) due to missing blood filter. Use as blood transfusion set without filter risks infection. Affected units sold in specific lots.
ICU MedicalAug 20, 2018 - Use cautionMedical device
NordicNeuroLab AS recalls fMRI Hardware System VisualSystem allows video signals from the stimulus presentation PC to enter the shielded scanner
NordicNeuroLab recalls fMRI hardware power supplies (LPS 1.0/1.1) that may drag into MRI scanner, causing injury. Affected units have specific serial numbers.
NordicNeuroLabAug 20, 2018 - Use cautionMedical device
Varian Medical Systems recalls VitalBeam Radiotherapy Delivery System Version 2.5 Product Usage: The VitalBeam delivery systems are intended to
Varian recalls VitalBeam radiotherapy systems version 2.5 due to potential treatment errors when patients with respiratory gating are moved between systems. Affected units have specific model numbers and were sold with certain software versions.
VarianAug 20, 2018 - UnratedDrug
RemedyRepack Inc. recalls Amlodipine/Valsartan/HCTZ 10mg/320mg/25mg Tablet, Rx Only (HDPE 90cc Bottles in cardboard trays) MFG Torrent Pharma
RemedyRePack recalls 10mg/320mg/25mg Amlodipine/Valsartan/HCTZ tablets (Rx only) due to trace NDMA impurity detected in manufacturing. Consumers should contact the company for details.
RemedyRePackAug 20, 2018 - Lower riskDrug
Hetero Labs Limited Unit V recalls Montelukast Sodium Tablets, 10 mg*, 30-count bottles, Rx Only, By: Hetero, Hetero Labs Limited, Unit V, Polepally,
Hetero Labs Limited recalls 10mg Montelukast Sodium tablets with blue specks. This may affect prescription medication safety. Stop using and contact your pharmacist.
Hetero Labs LimitedAug 20, 2018 - Use cautionFood
Ochoa's Queseria LLC recalls Mexican Style Ricotta Cheese labeled, "Don Froylan Requeson***Mexican Style Ricotta Cheese***Ingredients: Pasteurized
Ochoa's Queseria recalls Mexican Style Ricotta Cheese that does not list milk as an ingredient, a major food allergen. The product contains pasteurized whey from whole milk but fails to declare milk.
Ochoa's QueseriaAug 20, 2018 - Stop using nowFood
Portland Chocolate Company LLC recalls 60% Dark Chocolate Chips, packaged in poly-lined cardboard boxes, net wt. 30 lbs. The label is read in parts: "***
Portland Chocolate Company recalls 3450 lbs of 60% Dark Chocolate Chips due to peanut cross-contamination. Check your bulk containers.
Pitch Dark ChocolateAug 18, 2018 - Stop using nowFood
Air Stream Corp. recalls Shredded green cabbage
Air Stream Corp. recalls lot 5818-1 of shredded green cabbage due to potential Listeria monocytogenes contamination. Check your fridge and discard if affected.
Air Stream Corp.Aug 18, 2018 - Use cautionVehicle
WINNEBAGO INTENT (2018) recall — Structure
Winnebago is recalling 2018-2019 Intent vehicles due to potential mirror detachment. This could distract drivers and increase crash risk. Owners will receive free mirror security screws.
WinnebagoAug 17, 2018 - Use cautionVehicle
WINNEBAGO VIEW (2019) recall — Electrical System
Winnebago is recalling 2016-2019 View motorhomes with un-fused solar charging circuits. Unprotected circuits can overheat and cause fire if solar panels exceed amperage capacity. Owners must have a 15-amp fuse installed by dealers.
WinnebagoAug 17, 2018
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83,500 recalls tracked · 71,978 explained in plain English · 10,966 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.