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 cautionMedical device
Becton Dickinson & Company recalls SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696
Becton Dickinson recalls SmartSite Syringe Administration Sets (50-pack) due to leaking risk, which may cause infusion delays, under-infusion, or contamination. Affected units have specific catalog and lot numbers.
Becton DickinsonFeb 28, 2019 - Use cautionMedical device
Philips North America, LLC recalls MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application
Philips recalls MultiDiagnost-Eleva imaging systems with product codes 708032 and 708036 due to potential missing locking plate causing uncontrolled table tilt during medical procedures.
PhilipsFeb 28, 2019 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg, a) 30 count (NDC 59746- 758-30) & b) 90 count (NDC
Jubilant Cadista recalls 150mg BuPROPion XL tablets with failed dissolution specs. These tablets may not release medication properly. Stop using and contact for details.
Jubilant CadistaFeb 28, 2019 - Lower riskDrug
Torrent Pharma Inc. recalls Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/12.5mg, a) 30-count (NDC: 13668-117-30), b) 90-count (NDC:
FDA-confirmed impurity in Torrent's Losartan Potassium/Hydrochlorothiazide tablets may exceed safe levels. Recalled lots from 2020 with specific NDC numbers.
TorrentFeb 28, 2019 - Lower riskDrug
Camber Pharmaceuticals Inc recalls Losartan Potassium Tablets USP, 50 mg, Rx only, a) 30 count (NDC 31722-701-30), b) 90 count (NDC 31722-701-90), c) 1000
Camber Pharmaceuticals recalls 50mg Losartan Potassium Tablets due to trace amounts of NMBA detected in the active ingredient. This may pose a contamination risk during medication use.
Camber PharmaceuticalsFeb 28, 2019 - Lower riskFood
Fungi Perfecti LLC recalls Host Defense MycoBotanicals Blood Sugar, dietary supplement, 500mg capsules, 60 ct per bottle, serving size 2 capsules
Fungi Perfect: Host Defense Blood Sugar dietary supplement (60 capsules) recalled due to undeclared wheat. Consumers should check product labels for gluten-free claim and verify UPC codes.
Fungi PerfectiFeb 28, 2019 - Use cautionConsumer product
Clinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
Clinical Resolution Laboratory recalls Numb 100 Topical Anesthetic Cream due to non-child-resistant packaging. Risk of poisoning to young children if ingested or applied. Consumers should stop using and contact for refund or replacement.
Clinical Resolution LaboratoryFeb 28, 2019 - Use cautionConsumer product
Biotouch Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
Biotouch recalls EZY Gel Topical Anesthetic due to non-child-resistant packaging. Risk of poisoning for young children. Consumers should remove from reach and contact for refund.
BiotouchFeb 28, 2019 - Use cautionVehicle
FREIGHTLINER SPRINTER 3500 (2016) recall — Equipment Adaptive/Mobility
Recall of 2016 Freightliner Sprinter 3500 vehicles with Ricon wheelchair lifts due to risk of wheelchair user tipping into vehicle during exit. Affected owners must contact Ricon or Midway for free replacement of lift cam.
MidwayFeb 27, 2019 - Use cautionVehicle
TRIUMPH STREET TWIN (2017) recall — Electrical System
Triumph recalls 2017 Street Twin motorcycles with electrical system issues that may cause headlight or indicator failure and engine stalling, increasing crash risk. Owners must get free updated clutch cable and harness replacement.
TriumphFeb 27, 2019 - Use cautionVehicle
LEXUS LS (2018) recall — Tires
Toyota is recalling 2018 Lexus LS vehicles with run-flat tires that may have a cracked reinforcement layer, causing tread separation and handling risks. Owners can get free tire replacements.
LexusFeb 27, 2019 - Use cautionVehicle
FREIGHTLINER CASCADIA (2019) recall — Service Brakes, Air
Daimler Trucks North America recalls 2018-2019 Freightliner Cascadia trucks with ABS warning light that may not reactivate after restarting. This could cause crashes. Owners must contact DTNA for free reprogramming.
Daimler Trucks North AmericaFeb 27, 2019 - Use cautionVehicle
BMW X7 (2019) recall — Seats
BMW recalls 2019 X7 models with business lounge seats due to potential improper bolt tightening that could increase crash injury risk. Owners may get free seat adapter bolts replaced.
BMWFeb 27, 2019 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Service Brakes, Air
Daimler Trucks North America recalls 2019-2020 Thomas Built Saf-T-Liner C2 school buses that may lack Anti-Lock Braking System modules, risking crashes without ABS.
Thomas Built BusesFeb 27, 2019 - Stop using nowVehicle
FREIGHTLINER CASCADIA (2020) recall — Electrical System
Daimler Trucks North America recalls certain 2020 Freightliner Cascadia trucks due to an instrument cluster error that may cause unexpected vehicle movement.
FreightlinerFeb 27, 2019 - UnratedMedical device
Cypress Medical Products LLC recalls McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,
Cypress Medical Products recalls McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Tests (part numbers 178-CK30T, 178-CT30, etc.) due to FDA CLIA waiver denial from packaging similarities to domestic products.
Cypress Medical ProductsFeb 27, 2019 - Lower riskMedical device
Teleflex Medical recalls Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500
Teleflex Medical recalls one piece male external catheters with incorrect sterile labeling. The device is not meant to be sterile in normal use for incontinence management.
Teleflex MedicalFeb 27, 2019 - Use cautionMedical device
Zevex Incorporated (dba MOOG Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron
MOOG recalls 20-set infusion sets with leaking filter that could cause contamination. Stop using if you have model REF 340-4130, lots CF1819415-23615.
MOOG Medical DevicesFeb 27, 2019 - Use cautionMedical device
Brainlab AG recalls Spine & Trauma 3D Navigation 1.0 (subpart of the system Navigation Software Spine & Trauma 3D, Version 3.0 ) Intended
Brainlab recalls Spine & Trauma 3D Navigation 1.0 software due to potential navigation errors during surgery. Affected units may show incorrect instrument positions, risking surgical errors. Contact for remedy.
BrainlabFeb 27, 2019 - Stop using nowConsumer product
Harbor Freight Tools Recalls Propane Torches Due to Burn Hazard
Harbor Freight recalls Greenwood propane torches (SKUs 61589, 61595) due to burn hazards. Stop using immediately and return for a free replacement.
GreenwoodFeb 27, 2019 - Stop using nowConsumer product
Harbor Freight Tools Recalls 12V Rechargeable Flashlights Due to Overheating and Burn Hazards
Harbor Freight Tools recalls 80 Lumen : Overheating during charging can cause burns. Return for $5 gift card refund.
Harbor Freight ToolsFeb 27, 2019 - Stop using nowMeat & poultry
McAllen Cold Storage, Ltd. Recalls Siluriformes Fish Products Produced Without Benefit Of Inspection
McAllen Cold Storage recalls ~51,942 lbs of frozen Basa fillets produced without USDA inspection. Do not consume; discard or return.
McAllen Cold StorageFeb 26, 2019 - Stop using nowMeat & poultry
Sahlen Packing Company, Inc. Recalls Ready-To-Eat Deli Meat Products Due to Possible Foreign Matter Contamination
USDA FSIS recalls 13,224 pounds of ready-to-eat deli ham products that may contain plastic. Consumers are urged not to consume these items and should discard or return them to the store.
Sahlen PackingFeb 26, 2019 - Use cautionVehicle
FORD E-250 (2014) recall — Equipment Adaptive/Mobility
Recall of 2014 Ford E-250 vehicles with Ricon wheelchair lifts due to risk of wheelchair user tipping into vehicle when exiting lift platform.
New England WheelsFeb 26, 2019 - Use cautionVehicle
KEYSTONE ALPINE (2019) recall — Equipment
Keystone is recalling 2019 Alpine and High Country Montana trailers with cargo trays that may detach, risking injury. Owners should contact customer service for free fastener replacement.
KeystoneFeb 26, 2019 - Use cautionVehicle
INTERNATIONAL LT (2020) recall — Engine And Engine Cooling
Navistar recalls certain 2016-2020 International LT trucks with exhaust system code 07BKP/07BKR. Cracked exhaust brackets can cause tailpipe detachment during driving, increasing crash risk. Free replacement of brackets and tailpipes available.
NavistarFeb 26, 2019 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Abbott Alinity c Processing Module LN 03R67-01 - Product Usage: The Alinity c processing module is a fully automated
Abbott recalls Alinity c Processing Module LN 03R67-01 due to potential safety interlock failure when removing bulk solution bottles, which could lead to improper operation.
AbbottFeb 26, 2019 - Use cautionMedical device
Biomet 3i, LLC recalls CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number ILDAN3 - Product Usage: BIOMET3i Restorative products are
Biomet 3i recalls certain tin abutments 3.4mm (item ILDAN3) due to screw over-driving risk. Affected units have specific lot numbers. Stop using immediately to prevent damage.
Biomet 3iFeb 26, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Moxifloxacin Ophthalmic Solution USP, 0.5%, 3 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454
Lupin Pharmaceuticals recalls certain moxifloxacin eye drops due to impurities. Affected lots from July 2018 to December 2020 may pose health risks. Consumers should check product details and contact Lupin for guidance.
LupinFeb 26, 2019 - Stop using nowFood
The CF Sauer Company recalls MONARCH SOUTHERN BARBECUE SAUCE MADE WITH MUSTARD NET 128 FL OZ(1 GAL) 3.78L INGREDIENTS: WATER, HIGH FRUTOSE CORN
The CF Sauer Company is recalling Monarch Southern Barbecue Sauce because labels lack correct allergen declarations for soy and wheat. Check your lot numbers.
Monarch SouthernFeb 26, 2019
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