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
34,959 found- Use cautionVehicle
FORD F-250 SD (2019) recall — Latches/Locks/Linkages
Ford is recalling 2019 F-250 trucks with electric tailgate latches that may open unexpectedly, causing cargo to fall and create road hazards. Owners must contact Ford by January 20, 2020 for free repairs.
FordApr 12, 2019 - Use cautionVehicle
FORD EXPLORER (2020) recall — Fuel System, Gasoline
Ford is recalling 2020 Explorer vehicles with a risk of fuel leaks causing fire. Owners must have a protective sleeve installed by dealers to prevent leaks.
FordApr 12, 2019 - Stop using nowVehicle
FLEETWOOD BOUNDER (2020) recall — Equipment
REV is recalling 2020 Fleetwood Bounder motorhomes with damaged generator exhaust pipes that could allow carbon monoxide to enter the vehicle, risking injury or death. Owners must have the pipe inspected and replaced by dealers.
REVApr 12, 2019 - Use cautionVehicle
FLEETWOOD DISCOVERY (2020) recall — Electrical System
REV is recalling 2020 Fleetwood Discovery motorhomes with improperly secured wiring that could cause fire. Owners must have a dealer inspect and repair the harness for free by January 31, 2020.
REVApr 12, 2019 - Lower riskMedical device
TIDI PRODUCTS recalls Posey Connected Twice-As-Tough Cuffs
TIDI recalls Posey Connected Twice-As-Tough Cuffs with model numbers 2796 and 2797 that don't meet design specifications. Consumers should check their product details to see if they are affected.
TIDIApr 12, 2019 - Lower riskMedical device
Tecan US, Inc. recalls Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and
Tecan recalls Freedom EVO 200 lab equipment due to gas springs not being replaced within the specified interval, which could lead to improper function during routine laboratory tasks.
TecanApr 12, 2019 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard
Bard recalls WavelinQ 4F EndoAVF System due to potential magnetic deficiency in catheters, which may cause procedural delays and increased kidney risk for diabetic dialysis patients. Affected units include specific model and lot numbers.
BardApr 12, 2019 - Lower riskMedical device
Geistlich Pharma North America, Inc. recalls Geistlich Bio-Oss Pen, Sterile cancellous granules in an applicator, 1-2mm 0.5g, For single use only, Part Number 20126
Geistlich Pharma North America recalls Bio-Oss Pen (Part 20126) due to visible green plastic during unscrewing. Affected lots: 81700464, 81700811, 81800292, 81800866. No remedy stated in recall.
Geist: 20126Apr 12, 2019 - Use cautionMedical device
OMNIlife science Inc. recalls OMNIBotics iBlock Cutting Guide, 4146-1000 - Product Usage: The OMNIBotics iBlock Cutting Guide is a stainless-steel
OMNIlife recalls iBlock Cutting Guide 4146-1000 due to potential loosening during use. This surgical tool is used with robotic knee implants and may cause injury if not securely attached.
OMNIlifeApr 12, 2019 - Use cautionDrug
Teva Pharmaceuticals USA recalls Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in (a) 150 mL bottle (NDC 0093-4150-80) (b) 80 mL bottle
Teva Pharmaceuticals USA recalls specific lots of Amoxicillin for Oral Suspension USP because assay results were below specification limits.
Teva PharmaceuticalsApr 12, 2019 - UnratedDrug
CMC Enterprise Pharmacy recalls Chlorothiazide 100 mg, 3.57 mL syringe, Made by: Enterprise Pharmacy, 4400 Golf Acres Drive, Bldg. J Suite E,
Enterprise Pharmacy recalls 100 mg chlorothiazide syringes with potential lack of sterility. Affected lots expired by April 2019. Consumers should check lot numbers and contact pharmacy for details.
Enterprise PharmacyApr 12, 2019 - Lower riskFood
Wawa, Inc. recalls Wawa Iced Tea Less Sugar, Net weight/number of units per package: 12 FL OZ. , Package type: Bottle Units per case: 24,
Wawa recalls 12 fl oz bottles of Iced Tea Less Sugar (expiring April 29, 2019) due to missing phenylketonuria warning and aspartame listing.
WawaApr 12, 2019 - Lower riskFood
Hilmar Cheese Company, Inc. recalls Colby Jack Cheese in 40 pound and 640 pound blocks
Hilmar recalls Colby Jack cheese blocks (40lb and 640lb) with foreign material. Consumers should check batch numbers 1001914855-1001914952 for affected products.
HilmarApr 12, 2019 - Lower riskFood
Caito Foods LLC. recalls Fresh cut watermelon, fresh cut honeydew melon, fresh cut cantaloupe and fresh cut mixed fruit containing one of these
Caito Foods recalls fresh cut watermelon, honeydew melon, cantaloupe and mixed fruit with Salmonella Carrau risk. Products best by or use by 4/19/2019 or earlier.
Caito FoodsApr 12, 2019 - Stop using nowConsumer product
Fisher-Price Recalls Rock 'n Play Sleepers Due to Reports of Deaths
Fisher-Price recalls all Rock 'n Play Sleepers after reports of infant deaths from rolling while unrestrained. Consumers must stop using and get a refund or voucher.
Fisher-PriceApr 12, 2019 - Use cautionVehicle
WESTERN STAR 4900 (2020) recall — Visibility
Daimler Trucks North America recalls 2016-2020 Western Star 4900 and 5700 trucks with sleeper cab vent windows that may detach while driving, creating road hazards.
Daimler Trucks North AmericaApr 11, 2019 - Use cautionMedical device
Intuitive Surgical Inc recalls da Vinci X Surgical System, IS4200 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three main
Intuitive Surgical recalls da Vinci Xi surgical systems (IS4000) with high friction in universal surgical manipulators causing resistance, hesitation, and jerking during use. Affected units have specific serial numbers and UDI codes.
Intuitive SurgicalApr 11, 2019 - Lower riskMedical device
NxStage Medical, Inc. recalls NxStage PureFlow B Solution, REF RFP-401, M535RPF4010 NxStage PureFlow B Solution is indicated for use with renal
NxStage recalls specific lots of PureFlow B Solution (Q1811789 & Q1811790) due to mislabeling. This could lead to incorrect product use in hemodialysis. Affected users should check their lot numbers.
NxStageApr 11, 2019 - Lower riskMedical device
Ethicon Endo-Surgery Inc recalls Straight Intraluminal Staplers, 25 mm diameter, Model SDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are
Ethicon recalls Straight Intraluminal Staplers (Model SDH25A) due to potential incomplete staple formation. Affected units were sold between February 2023 and March 2024. Consumers should contact Ethicon for details.
EthiconApr 11, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Divalproex Sodium Extended-Release Tablets, USP, 250 mg a) 100-count bottle (NDC 55111-0533-01), b) 500-count bottle
Dr. Reddy's recalls 250mg Divalproex Sodium Extended-Release Tablets due to packaging humidity exposure. These tablets may degrade in high humidity, affecting safety.
Dr. Reddy'sApr 11, 2019 - Lower riskFood
Makzemo LLC recalls BALQEES SPICES, Yemeni Spices Mix, NET WEIGHT: 230g (1/2 lb.) and 454 grams (1lb.) clear plastic container and 5 lbs.
Makzemo LLC recalls Yemeni Spices Mix products due to high lead levels. Consumers should avoid using these spices to prevent potential health risks from lead exposure.
MakzemoApr 11, 2019 - Lower riskFood
Patagonia Provisions Inc recalls Patagonia Provisions Classic Barbecue Savory Seeds; 1 oz. poly-film pouches. 12 units per case Vegan, Gluten Free
Patagonia Provisions recalls 12 units of Classic Barbecue Savory Seeds pouches due to gluten contamination exceeding 20 ppm. Products labeled gluten-free but contain gluten in finished goods. Consumers should check lot codes and contact for details.
Patagonia ProvisionsApr 11, 2019 - Use cautionConsumer product
Specialized Recalls Bicycles with Steerer Tube Collars Due to Fall and Injury Hazards
Specialized recalls select Roubaix, Ruby, Diverge, and Sirrus bicycles from 2017-2019 with steerer tube collars that can crack due to corrosion, causing loss of steering control and fall risks.
SpecializedApr 11, 2019 - Stop using nowConsumer product
DICK'S Sporting Goods Recalls Hunters' Tree Stands Due to Fall Hazard
DICK'S Sporting Goods recalls Field & Stream Timberline Hang On tree stands due to weld failure. Stop using immediately and return for a refund.
Field & StreamApr 11, 2019 - Stop using nowMeat & poultry
Yoakum Packing Co. Recalls Venison Sausage Products Due to Mislabeling
Yoakum Packing Co. recalls ~12,388 lbs of smoked venison sausage due to mislabeling containing undeclared pork. Do not consume.
Yoakum Packing Co.Apr 10, 2019 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Structure
Blue Bird is recalling certain 2019-2021 All American school buses due to insufficient roof rivets that could separate in crashes, risking injury. Owners must contact Blue Bird for free roof joint repairs.
Blue BirdApr 10, 2019 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Seats
Daimler Trucks North America recalls 2020 Thomas Built Buses Saf-T-Liner C2 school buses with seats that may not absorb crash impacts enough, risking injury. Owners must get free seat repairs by dealers.
Thomas Built BusesApr 10, 2019 - Lower riskMedical device
Becton Dickinson & Company recalls MaxZero Extension Sets with Needle-less Connector, Product codes MZ1000 MZ1000-07 MZ5301 MZ5302 MZ5303 MZ5304 MZ5305
Becton Dickinson recalls MaxZero Extension Sets with Needle-less Connector due to fluid droplets separating after disconnection. Affected product codes include MZ1000 through MZ9329 and others. No remedy specified in recall notice.
Becton DickinsonApr 10, 2019 - Use cautionMedical device
Stryker Neurovascular recalls Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only,
Stryker Neurovascular recalls AXS Vecta 71 Aspiration Catheters (Catalog # INC-11129-115, 125, 132) due to potential breakage or kinking if improperly removed from packaging or during use. Affected units have a use-by date of 2021-11-29.
Stryker NeurovascularApr 10, 2019 - Lower riskMedical device
Uromedica Inc. recalls ProACT Implantation Instrument Set, is a reusable, steam sterilizable surgical instrument set consisting of a U-Channel
Uromedica recalls ProACT Implantation Instrument Set (Model 750041, Lot UM00650) due to potential U-channel sheath damage to implant devices during use. Affected units may cause device damage when passed through sheaths.
Uromed: ProACTApr 10, 2019
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