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
35,025 found- UnratedDrug
Akorn, Inc. recalls TheraTears Extra (sodium carboxymethylcellulose) 0.25% Lubricant Eye Drops, 30 Sterile Single-Use Vials per box, Akorn
Akorn recalls TheraTears Extra lubricant eye drops due to lack of sterility assurance. This may pose infection risks if used improperly.
AkornSep 8, 2021 - Lower riskFood
Seabear Company recalls Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and Dominique Seafoods, packaged in
Seabear Company recalls Banquet Cut Cold Smoked Salmon (Item 2-92845) due to potential C. botulinum growth. Consumers should check pouch labels for production codes and thawing instructions.
Seabear CompanySep 8, 2021 - Use cautionVehicle
NISSAN ROGUE SPORT (2021) recall — Structure
Nissan recalls 2021 Rogue Sport vehicles with liftgate hinges that can separate in rear crashes, risking injury. Owners must have hinges replaced free by dealers.
NissanSep 7, 2021 - Use cautionVehicle
HYUNDAI SONATA (2021) recall — Fuel System, Gasoline
Hyundai recalls 2021 Sonata vehicles with fuel leaks that could cause fire. Owners must have fuel pipe inspected or replaced free by dealers.
HyundaiSep 7, 2021 - Use cautionVehicle
COACHMEN MIRADA (2020) recall — Equipment
Forest River recalls 2020 Coachmen Mirada RVs with Hehr 6400 Series windows due to adhesive failure that may cause window vent to detach, increasing crash risk. Free window replacement available.
Forest RiverSep 7, 2021 - Use cautionMedical device
DJO, LLC recalls Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following
DJO recalls 1-gallon Ultra-Myossage Lotion bottles (REFs 4262 and 4210) due to potential bacterial contamination. FDA issued a warning on August 18, 2021.
DJOSep 7, 2021 - Lower riskMedical device
W L Gore & Associates, Inc. recalls Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF BXAL085902E, 8 MM X 59 MM 8 Fr, LARGE BALLOON
W L Gore recalls specific heparin stents due to incorrect labeling that may contain a larger size than listed. Affected units have serial numbers starting with 22753580.
W L GoreSep 7, 2021 - Lower riskMedical device
NOX MEDICAL recalls Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.
NOX Medical recalls T3s recorders with firmware error causing inaccurate device position detection during sleep monitoring. Affected units have specific serial numbers. No action required as the issue does not pose a safety risk.
NOX MEDICALSep 7, 2021 - Stop using nowFood
De Wafelbakkers, LLC recalls De Wafelbakkers 18 ct Buttermilk Pancakes NET WT 1 lb. 8.7 oz. (703g) KEEP FROZEN packaged in clear flexible plastic
De Wafelbakkers recalls 18 ct frozen buttermilk pancakes due to potential Listeria monocytogenes contamination. Check your freezer for affected lots.
De WafelbakkersSep 7, 2021 - Use cautionFood
Baker's Corner Bakery recalls Oatmeal Cranberry Cookie, packed in closed bags, 12oz net wt. The label of affected product is read in parts:
Baker's Corner Bakery recalls 12oz Oatmeal Cranberry Cookies due to undeclared soybean oil. Check your pantry for affected lots distributed in WA.
Baker's Corner BakerySep 7, 2021 - Use cautionVehicle
SPARTAN GLADIATOR (2020) recall — Equipment
Four Guys recalls one 2020 Spartan Gladiator firetruck with a wireless remote that may not work due to battery drain. Owners must return the remote for a free software update.
Four GuysSep 6, 2021 - Lower riskFood
Velvet Ice Cream Company recalls Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case
Velvet Ice Cream Company recalls Raspberry Fudge Cordial 1.75 quarts due to undeclared allergen. Consumers should check UPC 070682100497 and Julian Date 19521 for affected lots.
Velvet Ice CreamSep 6, 2021 - Use cautionVehicle
YAMAHA XC155 (2018) recall — Engine
Yamaha recalls 2015-2020 XC155 scooters due to a primary sheave nut that may loosen and cause engine stall, increasing crash risk. Owners must stop riding until fixed.
YamahaSep 4, 2021 - Use cautionVehicle
KEYSTONE BULLET (2020) recall — Structure
Keystone is recalling 2020-2021 Bullet 34BIPR trailers with potentially incorrect emergency window handles that could be difficult to open in an emergency.
KeystoneSep 4, 2021 - Use cautionVehicle
RAM PROMASTER CITY (2020) recall — Service Brakes, Hydraulic
Chrysler recalls 2020-2021 RAM ProMaster City vehicles with faulty ABS modules that could cause loss of braking performance or autonomous braking functions.
ChryslerSep 3, 2021 - UnratedMedical device
Welch Allyn Inc Mortara recalls ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Model Numbers:
Welch Allyn recalls ELI 280 Resting Electrocardiographs with specific model numbers and software versions due to malfunction under certain operator workflows. No remedy stated in official notice.
Welch Allyn Inc MortaraSep 3, 2021 - Lower riskMedical device
Flower Orthopedics Corporation recalls Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Flower Orthopedics recalls EWK 201 bone fixation kit missing CDG 200 component. This could lead to improper bone fixation. Affected units sold with lot number 2104321637.
Flower OrthopedicsSep 3, 2021 - Lower riskMedical device
Roche Molecular Systems, Inc. recalls cobas EGFR Mutation Test v2-Somatic gene mutation detection system Catalog Number :07248563190
Roche recalls cobas EGFR Mutation Test v2 due to false mutation results for Ex20Ins mutations, potentially leading to incorrect cancer treatment decisions. Affected units include all lot numbers of the system.
RocheSep 3, 2021 - UnratedDrug
Meitheal Pharmaceuticals Inc recalls Glycopyrrolate Injection, USP 4mg per 20mL, 20 mL Multi-Dose Vials, Rx only, Mfd for Meitheal Pharmaceuticals, Chicago,
Meitheal Pharmaceuticals recalls 4mg per 20mL Glycopyrrolate Injection vials due to failed impurities and degradation. Affected lots expire Dec 2021-Apr 2022. Consumers should contact for details.
Meitheal PharmaceuticalsSep 3, 2021 - Stop using nowDrug
ICU Medical Inc recalls AMINOSYN II 15% An Amino Acid Injection, Sulfite-Free, 2000 mL in flexible containers, Rx ONLY, Hospira, Inc., Lake
ICU Medical recalls AMINOSYN II 15% amino acid injection due to particulate matter found in samples. This could cause serious issues for patients receiving the injection.
ICU MedicalSep 3, 2021 - UnratedDrug
Morton Grove Pharmaceuticals, Inc. recalls Promethazine With Codeine Oral Solution, (Promethazine Hydrochloride 6.25 mg/5mL & Codeine Phosphate 10 mg/5 mL), 1
Morton Grove Pharmaceuticals recalls 14,904 bottles of Promethazine With Codeine Oral Solution due to potential microbial contamination from contaminated sugar batches.
Morton Grove PharmaceuticalsSep 3, 2021 - Lower riskFood
Whole Foods Market Brand 365, Llc recalls Whole Foods Market - Vegan Croissant 4 Count CONTAINS WHEAT, SOY May contain other allergens due to shared production
Whole Foods Market recalls vegan croissants due to undeclared milk and egg allergens from shared production areas. Consumers should check packaging for the specific batch.
Whole Foods MarketSep 3, 2021 - Lower riskMedical device
Deroyal Industries, Inc. Lafollette recalls DeRoyal Procedure Packs containing Smiths Medical NORMOFLO Irrigation Warming Set
DeRoyal recalls procedure packs with Smiths Medical NORMOFLO Irrigation Warming Sets due to potential aluminum ions leaching into warming fluids. Affected units include specific lot numbers from 2021-2025.
DeRoyalSep 2, 2021 - Lower riskMedical device
BioMerieux SA recalls MYLA Versions: 4.7, 4.7.1, 4.8, 4.8.1 and 4.8.2, part of the VIRTUO System
BioMerieux recalls MYLA software versions 4.7 through 4.8.2 for potential false negative results in testing. Affected users should contact the company for updates.
BioMerieuxSep 2, 2021 - Lower riskMedical device
Elekta, Inc. recalls MOSAIQ Oncology Information System
Elekta recalls MOSAIQ Oncology Information System software version 2.83 where drug strength settings may revert to original after ordering changes. Affected units run with First Data Bank (FDB) and have specific UDI/GTIN numbers.
ElektaSep 2, 2021 - Lower riskMedical device
Medtronic Sofamor Danek USA Inc recalls Endoskeleton" TCS Interbody System with Titan nanoLOCK" Surface Technology, NanoLock, 6 Deg, Interbody, Medium, 10mm
Medtronic Sofamor Danek recalls Endoskeleton TCS Interbody System with Titan nanoLOCK Surface Technology due to possible mismatch between implant engraving and pouch labels. Affected units may require verification of labels before use.
Medtronic Sofamor DanekSep 2, 2021 - Lower riskMedical device
Abbott Molecular, Inc. recalls Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
Abbott recalls Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) due to potential false positive results. Affected units have specific lot numbers and expiration dates. Consumers should check their kit details.
AbbottSep 2, 2021 - Lower riskMedical device
W L Gore & Associates, Inc. recalls REF/Catalogue Number GSX0030H, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery
W L Gore recalls Cardioform Septal Occluder 30mm with 3-year expiration label instead of 2-year. Product sold outside US with specific serial numbers.
W L GoreSep 2, 2021 - Lower riskDrug
RISING PHARMACEUTICALS recalls Meclizine HCl Tablets, 25 mg, packaged in 100-count HDPE bottle, Distributed by: Rising Pharma Holdings, Inc. East
Rising Pharmaceuticals recalls 25mg Meclizine HCl tablets with incorrect labeling instructions. Consumers should check product details and contact the company for guidance.
Rising PharmaceuticalsSep 2, 2021 - Use cautionDrug
New Vision Pharmaceuticals LLC recalls CVS Health Daytime Severe Cold & Flu Relief Single-Use Vials Mixed Berry Flavor 8 Pre-Measured Vials 0.51 FL OZ (15 mL)
CVS Health recalls Daytime Severe Cold & Flu Relief vials due to subpotent drug levels. Check lot numbers and expiration dates for affected units.
CVS HealthSep 2, 2021
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