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
35,021 found- Use cautionMedical device
GA HEALTH COMPANY LIMITED recalls ScopeValet Guardian Disposable Endoscope Valves Set Distributed By Ruhof Corporation, 393 Sagamore Avenue, Mineola, NY
GA Health recalls ScopeValet Guardian Disposable Endoscope Valves Sets with sticky/broken suction buttons that may cause prolonged procedures. Affected units include specific product codes and lot numbers.
GA HealthNov 3, 2020 - Lower riskMedical device
Boston Scientific Corporation recalls EKOS Control System (CU) 4.0. UPN 600-40500 The EkoSonic MACH4 Endovascular (EKOS) System consists of a single use
Boston Scientific recalls EKOS Control System CU 4.0 units with older RF board design that may fail at low temperatures. Affected units have specific serial numbers listed in the recall notice.
Boston ScientificNov 3, 2020 - Lower riskDrug
Hikma Pharmaceuticals USA Inc. recalls Sodium Chloride Injection, USP, 0.9%, 0.308 mOsmol/mL, 2mL Single Dose Vial, Preservative Free, For use as a sterile
Hikma Pharmaceuticals recalls 0.9% Sodium Chloride Injection vials with failed pH tests. These products may not meet USP standards and could cause issues if used in medical procedures.
Hikma PharmaceuticalsNov 3, 2020 - Use cautionDrug
Teligent Pharma, Inc. recalls Triamcinolone Acetonide Lotion USP, 0.025%, 60 mL (60 grams) bottle, Rx Only, Teligent Pharma, Inc. Buena, New Jersey
Teligent Pharma recalls one lot of Triamcinolone Acetonide Lotion USP, 0.025% because it does not meet assay results for potency.
Teligent PharmaNov 3, 2020 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Power Train
Blue Bird recalls 2018-2019 school buses with electric drivetrains due to risk of sudden power loss causing crashes. Owners must contact Blue Bird or Cummins for free cable tie fix.
Blue BirdNov 2, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft
Smith & Nephew recalls bone fixation nails (TRIGEN INTERTAN) with model numbers 71675535 and 71675532 due to manufacturing packaging error. Affected units may have incorrect labeling.
Smith & Neph: Inc.Nov 2, 2020 - Lower riskMedical device
Chromsystems Instruments & Chemicals GmbH recalls MassChrom Amino Acid Analysis Plasma Control Level I, Order No. 0471 - Product Usage: The kit is intended for amino
Chromsystems recalls MassChrom Amino Acid Analysis Plasma Control Level I kits that may impact test results due to stability issues. Affected kits have Order No. 0471 and Lot No. 2019 (expiring 05/01/2022).
ChromsystemsNov 2, 2020 - Lower riskMedical device
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage: intended to be used only with various
Respironics California, LLC
Respironics California, LLCNov 2, 2020 - UnratedDrug
Preferred Pharmaceuticals, Inc. recalls Metformin HCl Extended Release Tablets USP 500 mg, Generic for : Glucophage XR, Pkg Size 100, Mfg: Time-Cap Labs, Inc.;
Preferred Pharmaceuticals recalls Metformin HCl Extended Release Tablets (Glucophage XR) due to excessive N-Nitrosodimethylamine (NDMA) detected in some batches. This chemical poses a potential cancer risk. Consumers should check their product details and contact the company for instructions.
Preferred PharmaceuticalsNov 1, 2020 - Use cautionVehicle
MERCEDES-BENZ AMG E53 (2021) recall — Seats
Mercedes-Benz recalls 2021 AMG E53 vehicles with front passenger seats that may not have a mechanical adjustment limit, increasing injury risk during airbag deployment. Owners should contact MBUSA for free seat inspections.
Mercedes-BenzOct 30, 2020 - Stop using nowVehicle
KEYSTONE COUGAR (2020) recall — Equipment
Keystone recalls certain 2020-2021 Cougar trailers with Off the Grid solar packages due to inverter wiring issues that may energize shore power connections.
KeystoneOct 30, 2020 - Stop using nowMedical device
Invacare Corporation recalls Invacare PerfectO2 V Oxygen Concentrator- intended for patients with respiratory disorders requiring supplemental
Invacare recalls PerfectO2 V oxygen concentrators due to fire or cap explosion risks from internal valve failures. Affected models include IRC5PO2V (US) with specific serial numbers. Contact Invacare for remedy.
InvacareOct 30, 2020 - Lower riskMedical device
Neocis, Inc. recalls DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis
Neocis recalls Gen 2 Anterior Chairside Splints due to possible mislabeling. Affected units may not be correctly identified, but no safety risk is reported.
NeocisOct 30, 2020 - Lower riskMedical device
Luminex Corporation recalls Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
Luminex recalls Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model 20-006-024 due to potential false-negative results. Consumers should check product codes for affected units.
LuminexOct 30, 2020 - Lower riskMedical device
Respironics California, LLC recalls Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only with various
Philips Respironics recalls V60 Ventilator model 1053615 due to potential backup battery failure if over-discharged or stored without AC power. Affected units have specific serial numbers listed.
Philips RespironicsOct 30, 2020 - Lower riskDrug
AVKARE Inc. recalls Mesalamine Delayed-Release Tablets, USP 1.2 gram (Once-Daily), 120 Tablets bottle, Rx Only Manufactured for: AvKARE,
AVKARE recalls 120-tablet mesalamine delayed-release tablets (Rx only) due to failed dissolution specifications. This may affect tablets with NDC 42291-564-12 and specific expiration dates.
AVKAREOct 30, 2020 - Use cautionVehicle
JAYCO NORTHPOINT (2021) recall — Suspension
Jayco is recalling certain 2020-2021 Northpoint 387RDFS(LZ) trailers due to potential wheel spindle failure causing crash risk. Owners should contact Jayco for free axle inspection.
JaycoOct 29, 2020 - Use cautionVehicle
TRIPLE E UNITY (2020) recall — Equipment
Triple E recalls 2020 Unity motorhomes with incorrect propane connector that may leak propane, causing fire risk. Free replacement of faulty connector available.
Triple EOct 29, 2020 - Use cautionVehicle
ENTEGRA VISION (2020) recall — Engine
Jayco is recalling 2020-2021 Entegra Vision motorhomes due to potential excessive interior heat from engine covers, which could cause injury. Owners must contact Jayco for free repairs.
JaycoOct 29, 2020 - Use cautionVehicle
BUICK ENCORE (2020) recall — Power Train
GM recalls 2020 Buick Encore vehicles with missing bolts on start-stop accumulator endcap, risking transmission oil leaks, loss of propulsion, and potential fire. Owners must have dealers inspect and replace the component.
BuickOct 29, 2020 - Stop using nowVehicle
BMW M4 (2020) recall — Fuel System, Gasoline
BMW recalls certain 2020 M4 Coupes due to a fuel leak risk. Dealers will inspect and replace parts free of charge if a damping component is missing.
BMWOct 29, 2020 - Use cautionMedical device
Prytime Medical Devices, Inc. recalls PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths,
Prytime Medical recalls ER-Reboa Plus Catheters with potential incorrect balloon marking, risking procedure delays or patient injury. Affected units have specific model and lot numbers.
Prytime MedicalOct 29, 2020 - Lower riskMedical device
Chromsystems Instruments & Chemicals GmbH recalls 6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used
Chromsystems recalls specific lots of 6PLUS1 Multilevel Saliva Calibrator Sets due to potential inaccurate cortisol and cortisone test results. Affected units may need replacement.
ChromsystemsOct 29, 2020 - Use cautionConsumer product
Serena & Lily Recalls Nash Convertible Cribs Due to Injury Hazard (Recall Alert)
Serena & Lily recalls Nash Convertible cribs due to risk of leg detachment from headboard and footboard, potentially causing injury. Affected units sold with specific PO numbers and dates; consumers can repair, replace, or get a refund.
Serena & LilyOct 29, 2020 - Stop using nowConsumer product
Mueller Austria Recalls Onion Choppers Due to Serious Laceration Hazard
Mueller Austria recalls onion choppers with a locking tab that can detach, causing hand injuries. Consumers must stop using and get a free replacement with improved safety.
Mueller AustriaOct 29, 2020 - Stop using nowConsumer product
Gorilla Commerce Recalls Oven Liners Due to Risk of Carbon Monoxide Poisoning (Recall Alert)
Gorilla Commerce recalls heavy-duty oven liners sold in sets of three due to risk of carbon monoxide poisoning if not properly installed. Consumers should stop using and contact for refunds.
Gorilla CommerceOct 29, 2020 - Use cautionVehicle
JAYCO ALANTE (2021) recall — Equipment
Jayco is recalling 2021 Alante RVs with Power Bedlift System due to risk of bed releasing while moving, potentially blocking driver vision and causing crashes. Owners must contact Jayco for free bed motor replacement.
JaycoOct 28, 2020 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 4500 (2020) recall — Steering
Mercedes-Benz Sprinter 4500 (2020) vehicles with power steering return line hoses that may detach and leak hydraulic fluid. Owners should contact DVUSA for free repairs to prevent crash risk.
Mercedes-BenzOct 28, 2020 - Stop using nowDrug
Lohxa LLC recalls Chlorhexidine Gluconate Oral Rinse USP, 0.12%, Alcohol Free, packaged in 15 mL unit does cups (barcode 7016602715),
Lohxa recalls 15mL alcohol-free chlorhexidine rinse due to Burkholderia lata contamination. Products with specific lot numbers and expiration dates are affected. Consumers should stop using and contact Lohxa for details.
LohxaOct 28, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Mesalamine Delayed-Release Tablets, USP 1.2 gram, 120 tablets per bottle, Rx Only, Manufactured by: Actavis
Teva Pharmaceuticals USA recalls specific lots of Mesalamine Delayed-Release Tablets due to failed dissolution testing. Consumers should contact the company for details.
Teva Pharmaceuticals USAOct 28, 2020
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