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
35,069 found- UnratedMedical device
Carl Zeiss Meditec, Inc. recalls CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Carl Zeiss Meditec recalls CIRRUS HD-OCT models 5000 AngioPlex and 6000 AngioPlex with unapproved optic nerve head angiography scans. Affected units have specific software versions and serial numbers.
Carl Zeiss MeditecJan 14, 2022 - Use cautionMedical device
Stryker Corporation recalls 1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear
Stryker recalls 1688 Camera Control Units with software defects causing image flips, risking surgical errors. Affected units have specific serial numbers and software versions.
StrykerJan 14, 2022 - Use cautionMedical device
Hill-Rom, Inc. recalls (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX
Hill-Rom recalls specific Traverse Rail Carrier models with potentially loose screws that could cause the rail system to fall, risking injury to caregivers and patients. Affected units include 3101704, 3102514, and other models sold between January 2021 and March 2021.
Hill-RomJan 14, 2022 - Lower riskMedical device
Sunstar Americas, Inc. recalls BUTLER Clear Dip, 12 bottles/case
Sunstar recalls Butler Clear Dip 12-bottle cases with specific SKUs due to lack of premarket clearance. Consumers should check their product details to determine if affected.
SunstarJan 14, 2022 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
Howmedica Osteonics recalls Biolox delta Ceramic V40 Femoral Heads 32/ +4.0mm (Catalog 6570-0-232) due to potential size/offset mismatch with labeling. Affected units may have incorrect dimensions for surgical use.
Howmedica OsteonicsJan 14, 2022 - Lower riskDrug
Mayne Pharma Inc recalls Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville,
Mayne Pharma recalls Lexette (halobetasol propionate) 0.05% topical foam canisters due to difficulty dispensing or dispensing liquid instead of foam. This is a CGMP deviation affecting certain lots.
Mayne PharmaJan 14, 2022 - Stop using nowDrug
Aurobindo Pharma USA Inc. recalls Moxifloxacin Ophthalmic Solution, USP 0.5% w/v, 3 mL bottle, Sterile, Rx Only, Distributed by: Aurobindo Pharma USA,
Aurobindo Pharma recalls 0.5% moxifloxacin eye drops due to impurities that could cause eye injury. Affected lots from India, expiring June 2023. Stop using immediately.
Aurobindo PharmaJan 14, 2022 - Use cautionVehicle
FORD FUSION (2015) recall — Service Brakes, Hydraulic
Ford is recalling 2015 Fusion vehicles with brake pedal bumpers that can corrode and separate, causing brake lights to stay on and increasing crash risk. Owners must contact Ford for free replacement.
FordJan 13, 2022 - UnratedMedical device
Nextremity Solutions recalls Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital
Nextremity Solutions recalls its Nextra CH Cannulated Hammertoe Mini Instrument Kit for potential surgical complications. The device may deform the implant locking mechanism during insertion, leading to delays or revision surgery.
Nextremity SolutionsJan 13, 2022 - Lower riskMedical device
Lusys Laboratories, Inc. recalls Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)
Lusys recalls its 2nd Gen COVID-19 antigen test kits as they lack U.S. FDA authorization. These kits may not be reliable for detecting the virus in the U.S. market.
LusysJan 13, 2022 - Lower riskMedical device
ROi CPS LLC recalls Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile
ROi CPS recalls Regard TOTAL HIP - SPRINGFIELD kits with incorrect labeling on individual kits. This mislabeling may cause confusion in surgical use. Affected kits have specific item and lot numbers.
ROi CPSJan 13, 2022 - Lower riskMedical device
K2M, Inc recalls Everest MI XT Inner Dilator, Catalog Number 5101-90167
K2M recalls Everest MI XT Inner Dilators (Catalog 5101-90167) due to improper fit during surgery. Affected units may not assemble correctly, risking surgical complications.
K2MJan 13, 2022 - Stop using nowMedical device
Physio-Control, Inc. recalls HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Physio-Control recalls HeartSine Samar: Defibrillators shipped without battery packs. Users must check serial numbers to confirm if affected. No remedy details provided in recall notice.
Physio-ControlJan 13, 2022 - Lower riskFood
Sugar Plum Inc. recalls Sugar Plum Vegetable Seasoning Blends Sesame Soy sold in the Veggie Lovers Cooking Kit. 1.5 oz packet. Packaged in a
Sugar Plum recalls Sesame Soy Vegetable Seasoning Blends sold in Veggie Lovers Cooking Kit due to undeclared wheat allergen. Affected products include 1.5 oz packets with UPC 745559665002.
Sugar PlumJan 13, 2022 - Lower riskFood
LILY'S SWEETS LLC recalls Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch
Lily's Sweets LLC recalls 7 oz. Peppermint Baking Chips pouches due to soy lecithin presence. Consumers should check product dates and contact the company for details.
Lily's SweetsJan 13, 2022 - Use cautionFood
Han Yang Corp. recalls Korean Sushi, net wt. 12 oz. UPC 0 72148 48043 3. The label is read in parts: "***KOREAN SUSHI ***Ingredients: Rice,
Han Yang Corp. recalls 61 packages of 12 oz Korean Sushi distributed in WA due to undeclared Yellow #5 allergen.
Han YangJan 13, 2022 - Use cautionConsumer product
Textron Specialized Vehicles Recalls Personal Transportation Vehicles (PTV), Due to Fall and Injury Hazards (Recall Alert)
Textron Specialized Vehicles recalls 2022 E-Z-GO Freedom RXV models with rear seats due to risk of unexpected rear seat tilting causing falls and injuries. Affected vehicles have serial numbers 5633701-5651753.
Textron Specialized VehiclesJan 13, 2022 - Use cautionDrug
Ascend Laboratories, LLC recalls Metoprolol Succinate Extended-Release Tablets, USP, 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: Alkem
Ascend Laboratories recalls 9,216 bottles of Metoprolol Succinate Extended-Release Tablets (25 mg) due to failed dissolution specifications.
Ascend LaboratoriesJan 12, 2022 - Lower riskFood
Natural Way Cheese recalls Natural Way Cheese Horseradish Cheese Curds, retail 12oz plastic bag UPC 8 10056 75106 7, 12 retail units per wholesale
Natural Way Cheese recalls horseradish cheese curds due to milk stored in holding tank over 72 hours, risking bacterial growth. Affected units sold April 2022.
Natural Way CheeseJan 12, 2022 - Stop using nowConsumer product
Giant Bicycle Recalls Bicycles Due to Fall and Injury Hazards
Giant recalls 2021 model year bicycles with loose handlebar stems that can cause falls and injuries. Affected models include Cypress DX, Escape 3 Comfort, Liv Flourish FS 1 and Alight 3 Comfort. Consumers must stop using and get free repairs.
GiantJan 12, 2022 - Stop using nowConsumer product
EGL Motor Recalls Youth All-Terrain Vehicles (ATVs) Due to Injury Hazard and Violation of Federal ATV Safety Standard
EGL Motor recalls youth ATVs (MADIX 125 and D110) due to injury risks from high-speed crashes and handlebar lacerations. Consumers must stop using and get repairs.
EGL MotorJan 12, 2022 - Stop using nowConsumer product
Children's Robes Recalled by HulovoX Due to Violation of Federal Flammability Standards and Burn Hazard
HulovoX recalls children's robes that fail flammability standards, risking burns to children. Affected robes were sold online in rainbow colors and sizes 3T-12. Consumers should stop using and return for refund.
HulovoXJan 12, 2022 - Use cautionVehicle
TESLA MODEL S (2021) recall — Steering
Tesla recalls 2021 Model S vehicles with potential steering power loss on rough roads or potholes. Owners must install free software update to prevent increased crash risk.
TeslaJan 11, 2022 - Use cautionVehicle
TESLA MODEL S (2021) recall — Visibility
Tesla is recalling 2021 Model S vehicles with specific rearview mirrors that may cause drivers to misjudge vehicle distances, increasing crash risk. Owners must have mirrors replaced free by Tesla.
TeslaJan 11, 2022 - Use cautionVehicle
FREIGHTLINER BUSINESS CLASS M2 (2020) recall — Service Brakes, Air
Daimler Trucks North America recalls 2020 Freightliner Business Class M2 trucks with brake modulator valves that may corrode, causing sudden vehicle pull during ACC braking. Free repairs to prevent crash risk.
Daimler Trucks North AmericaJan 11, 2022 - Lower riskMedical device
Diagnos Inc recalls CARA (Computer Assisted Retinal Analysis), Product ID: +B543CARA0/$$+7V4.7.2/16D202111179
Diagnos Inc recalls CARA retinal analysis software version 4.7.2 due to unapproved AI features. Users should revert to a prior software version to avoid potential risks.
DiagnosJan 11, 2022 - Use cautionMedical device
TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component:
Arrow recalls specific Percutaneous Thrombolytic Device kits (PTD) with potential tip separation during use. Affected units include certain lot numbers and model codes. Stop using immediately if you own these kits.
ArrowJan 11, 2022 - Lower riskDrug
Pharmasol Corporation recalls Lung Cleaner (saline eucalyptus) inhaler, 37 oz cans, Manufactured For: The Lung Cleaner LLC Boulder, CO 80302
Pharmasol Corporation recalls Lung Cleaner saline eucalyptus inhalers (37 oz cans) manufactured for The Lung Cleaner LLC in Boulder, CO due to cGMP deviations. Consumers should contact the company for details.
Pharmasol CorporationJan 11, 2022 - UnratedDrug
Exela Pharma Sciences LLC recalls 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), 50 mL vials, Rx Only, Manufactured and Distributed by:
Exela Pharma Sciences recalls 50mL sodium bicarbonate injection vials due to lack of sterility assurance. This medication is prescription-only and may pose infection risks if used.
ExelaJan 11, 2022 - Use cautionConsumer product
Residential Elevators Recalled by Savaria Corporation Due to Child Entrapment Hazard; Risk of Serious Injury or Death to Young Children
Savaria and Garaventa residential elevators (1999-2021) recalled due to child entrapment hazard. Risk of serious injury or death if young children get stuck between elevator doors.
SavariaJan 11, 2022
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