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
35,006 found- Use cautionVehicle
LANCE TRAVEL TRAILER (2020) recall — Equipment
Lance Camper is recalling certain 2018-2021 travel trailers with Dometic propane stoves due to potential gas leaks that could cause fire. Owners should contact customer service for free repairs.
Lance CamperJul 10, 2020 - Lower riskMedical device
RANDOX LABORATORIES, LTD. recalls Amylase AY3805 batch 480449 Amylase Ethylidene Blocked-pNPG7 Reagent
Randox recalls specific batches of Amylase Ethylidene Blocked-pNPG7 Reagent due to performance failures before expiry. Affected units may not function correctly as intended.
RandoxJul 10, 2020 - UnratedDrug
Keryx Biopharmaceuticals, Inc. recalls Auryxia (ferric citrate) tablets 210 mg, Rx Only, 200 tablets per bottle, Manufactured for and distributed by: Keryx
Keryx Biopharmaceuticals recalls Auryxia 210mg tablets due to FDA manufacturing process deviations. Affected lots were not made per approved standards. Consumers should contact Keryx for details.
KeryxJul 10, 2020 - Use cautionMedical device
Medline Industries Inc recalls Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are single use devices intended to clean the
Medline recalls endoscopic cleaning brushes DYK1002DCB and DYK10: Potential brush detachment during cleaning. Stop using immediately to prevent injury.
MedlineJul 9, 2020 - Lower riskMedical device
Mako Surgical Corporation recalls Mako Hip End Effector, Variable Angle Catalog Number: 206967 GTIN:00848486022167
Mako Surgical recalls variable angle hip end effectors with catalog number 206967 due to potential bone preparation discrepancies during hip surgery.
MakoJul 9, 2020 - Stop using nowDrug
Maquiladora Miniara Sa De Cv recalls Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl oz (1L) bottle, Made in Mexico By: Maquiladora Miniara
FDA recalls Shine & Clean Hand Sanitizer gel (1L) made in Mexico due to ethanol content below label claims and undeclared methanol presence. Consumers should stop using affected batches.
Maquiladora MiniaraJul 9, 2020 - Stop using nowConsumer product
RH Recalls Riveted Mesh Floor Lamps Due to Fire Hazard (Recall Alert)
RH recalls Riveted Mesh floor lamps due to fire hazard from overheating foot switches. Stop using immediately and contact RH for a full refund.
RHJul 9, 2020 - Use cautionConsumer product
Miracle Botanicals Recalls Wintergreen and Birch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Miracle Botanicals recalls wintergreen and birch essential oils due to non-child-resistant packaging. Risk of poisoning if young children swallow the product. Consumers should store out of reach and get free child-resistant caps.
Miracle BotanicalsJul 9, 2020 - Stop using nowConsumer product
DaVinci Recalls Bassinets Due to Fall and Entrapment Hazards (Recall Alert)
DaVinci recalls wooden Bailey bassinets for infants due to risk of fall and entrapment. Consumers must stop using and contact DaVinci for free repair kit.
DaVinciJul 9, 2020 - Stop using nowConsumer product
Cooper Lighting Recalls Light Fixtures Due to Injury Hazard (Recall Alert)
Cooper Lighting recalls field and prism RGBA light fixtures due to risk of lens separation causing injury. Affected models include ALL FIELD AF, AN, ST series and Prism RGBA PM series. Contact for free repair.
Cooper LightingJul 9, 2020 - Use cautionConsumer product
Ananda Apothecary Recalls Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Ananda Apothecary recalls wintergreen, sweet birch, super soother, and breathe deep essential oils due to non-child-resistant packaging, risking poisoning if young children swallow.
Ananda ApothecaryJul 9, 2020 - Stop using nowMeat & poultry
FSIS Issues Public Health Alert for Ready-To-Eat Diced Chicken Products Due to Misbranding and an Undeclared Allergen
BrucePac issued a public health alert for RTE diced chicken due to undeclared soy. Consumers who received these products are urged not to consume them.
BrucePacJul 8, 2020 - Use cautionVehicle
FREIGHTLINER BUSINESS CLASS M2 (2020) recall — Electrical System
Daimler Trucks North America recalls 2017-2021 Freightliner Business Class M2 trucks with potential engine harness damage causing stalls and crash risk. Free repairs available.
Daimler Trucks North AmericaJul 8, 2020 - Use cautionVehicle
BMW X5 (2020) recall — Power Train
BMW is recalling 2020 X5 models with a potential starter motor bolt that could fall into the transmission, causing engine stalls and crash risks. Free repairs available.
BMWJul 8, 2020 - Lower riskMedical device
Canon Medical System, USA, INC. recalls System Model: Ultimax-i, DREX-UI80 (DREX-UI80); Unit Model: HDR-08A Imager Processor; UDI (01)04987670100147
Canon Medical recalls Ultimax-i DREX-UI80 units with HDR-08A Imager Processor model where image counts differ from original during PACS transfer. Affected units have specific serial numbers listed in the recall notice.
Canon MedicalJul 8, 2020 - Lower riskMedical device
New Wave Endo-Surgical, Corp. recalls M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall
New Wave Endo-Surgical recalls M-Close Kit REF 27-101 due to risk of plastic housing fracturing. Affected units have UDI/DI 00850009417022 and lot code C2020.
New Wave Endo-SurgicalJul 8, 2020 - Lower riskMedical device
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Medium, Left, Catalog Number CPF 102 - Product Usage: intended to be used for internal
Flower Orthopedics recalls specific calcaneus plates made with incorrect titanium alloy. This may cause complications during bone repair. Affected units include catalog number CPF 102, lot numbers 1909660029 and 1909660031.
Flower OrthopedicsJul 8, 2020 - Stop using nowConsumer product
Pranarom Recalls Wintergreen Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning
Pranarom recalls wintergreen essential oils due to non-child-resistant packaging, posing poisoning risk for young children. Consumers must dispose of product and get free replacement.
PranaromJul 8, 2020 - Stop using nowConsumer product
Lidl US Recalls Silvercrest Bread Makers Due to Electric Shock Hazard
Lidl recalls Silvercrest bread makers with specific IAN codes due to electric shock risk from energized lids. Affected units must be unplugged and returned for refund.
LidlJul 8, 2020 - Use cautionConsumer product
GloryBee Natural Sweeteners Recalls GloryBee Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
GloryBee Wintergreen Essential Oil lacks child-resistant packaging, risking poisoning for young children. Consumers should store safely and get a free replacement cap.
GloryBeeJul 8, 2020 - Use cautionVehicle
DODGE NITRO (2011) recall — Air Bags
Chrysler recalls 2011 Dodge Nitro vehicles with loose steering wheel emblem that may become projectiles during airbag deployment, risking injury. Owners must contact FCA US LLC for free air bag cover replacement.
ChryslerJul 7, 2020 - Use cautionVehicle
AUDI S8 (2016) recall — Structure
Volkswagen recalls 2013-2018 Audi S8 vehicles with potential engine seal fire risk. Owners must contact Audi for a free retaining plate fix.
AudiJul 7, 2020 - Stop using nowVehicle
KEYSTONE FUZION (2020) recall — Equipment
Keystone recalls certain 2019-2020 Fuzion trailers due to a TV antenna that may detach while driving, creating a road hazard.
KeystoneJul 7, 2020 - Use cautionDrug
Mylan Institutional LLC recalls Daptomycin for Injection, 500 mg/vial, Single-Dose Vial, Rx only, Sterile, Manufactured for: Mylan Institutional, LLC,
Mylan recalls Daptomycin 500mg vials due to possible particulate matter. This could cause serious injury if injected. Affected vials have specific lot numbers and expiration dates.
MylanJul 7, 2020 - Use cautionDrug
CareFusion 213, LLC recalls ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution -
CareFusion recalls ChloraPrep With Tint 2% chlorhexidine solution for potential fungal growth in humid climates. Affected lots sold in Zone IV regions with specific expiration dates.
CareFusionJul 7, 2020 - Use cautionDrug
Lupin Pharmaceuticals Inc. recalls Metformin Hydrochloride Extended-release Tablets USP 500 mg, 100 count bottles, Rx only, Manufactured for: Lupin
Lupin Pharmaceuticals recalls 64,344 bottles of Metformin Hydrochloride Extended-release Tablets 500 mg due to N-Nitrosodimethylamine (NDMA) impurity.
LupinJul 7, 2020 - Lower riskFood
KIND LLC recalls ***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted Coconut***INGREDIENTS: Oats, tapioca syrup, brown rice, cane
KIND LLC recalls 11oz and 17oz pouches of Healthy Grains Oats & Honey Granola with Toasted Coconut due to undeclared sesame seeds. Check product lot numbers for affected items.
KINDJul 7, 2020 - Lower riskMedical device
Arrow International Inc recalls Cannon II Plus Replacement Hub Set - Product Usage: is indicated for use in the replacement of a Cannon II Plus hub
Arrow recalls Cannon II Plus Replacement Hub Set with incorrect expiration dates on labels. Using expired products may increase infection risk. Consumers should check product codes and contact Arrow for details.
ArrowJul 6, 2020 - Use cautionMedical device
Golden Technologies, Inc. recalls Golden Technologies Model Number PR515 Lift Chair - Product Usage: is to provide lift assistance for persons who have
Golden Technologies recalls PR515 Lift Chairs due to suspect poor weld on back KD bar. This could lead to structural failure during use. Affected units have model PR515 with UDI B247PR515.
Golden TechnologiesJul 6, 2020 - Lower riskMedical device
Sysmex America, Inc. recalls Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product Usage: is a fully automated, user
Sysmex recalls PS-10 Sample Preparation System with catalog number BQ716341 due to insufficient antibody causing errors without alarms. Affected units have specific serial numbers listed.
SysmexJul 6, 2020
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83,594 recalls tracked · 72,041 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.