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
35,004 found- Use cautionVehicle
WINNEBAGO ADVENTURER (2020) recall — Electrical System
Winnebago recalls 2017-2020 Adventurer motorhomes with electrical connector mounted on floor. Wet floor can cause electrical short and fire. Owners must have connector mounted on metal bracket by dealer.
WinnebagoNov 13, 2019 - Lower riskMedical device
Medtronic Xomed, Inc. recalls Lamicel 10PK 10MM INTL
Medtronic Xomed recalls Lamicel 10PK 10MM INTL due to inadequate sterilization. Affected units have specific UDI and lot numbers. Consumers should contact for details.
Medtronic XomedNov 13, 2019 - Use cautionMedical device
Linet Spol. S.r.o. recalls Eleganza 5 (AC powered adjustable bed), Item Numbers: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, and d)
Linet recalls Eleganza 5 AC-powered adjustable beds with specific item numbers due to potential side rail malfunction causing improper locking or sticking in upper position.
LinetNov 13, 2019 - Stop using nowMedical device
GETINGE US SALES LLC recalls Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion Membrane Oxygenator with Bioline Coating, Sterile
Getinge recalls pediatric oxygenators with potential sterile barrier compromise. Affected units have specific lot codes; stop use immediately if you own one.
GetingeNov 13, 2019 - UnratedDrug
Natures Rx recalls Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil
Natures Rx recalls 10-capsule male enhancement products containing undeclared sildenafil. Products marketed without FDA approval may pose health risks.
Natures RxNov 13, 2019 - UnratedDrug
Precision Dose Inc. recalls Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit
Precision Dose recalls ranitidine oral solution due to impurity N-nitrosodimethylamine (NDMA) found in the active pharmaceutical ingredient. This product is prescription-only and may pose health risks.
Precision DoseNov 13, 2019 - Stop using nowConsumer product
Mystery Ranch Recalls Holsters for Semi-Automatic Handguns Due to Injury Hazard (Recall Alert)
Mystery Ranch recalls semi-automatic handgun holsters due to retention strap disconnecting, causing guns to fall and discharge. Consumers must stop using and get refunds.
Mystery RanchNov 13, 2019 - Stop using nowVehicle
VOLKSWAGEN GOLF (2019) recall — Wheels
Volkswagen recalls 2019 Golf models with potentially faulty wheel bearings that could cause crashes. Owners must stop driving until repairs are made.
VolkswagenNov 12, 2019 - Use cautionVehicle
TOYOTA PRIUS (2019) recall — Electrical System
Toyota is recalling 2019 Prius vehicles with blank speedometer and fuel gauge due to electrical short circuit. This could cause crashes. Owners must contact Toyota for free repair.
ToyotaNov 12, 2019 - Use cautionVehicle
PORSCHE 911 GT3 (2019) recall — Equipment
Porsche recalls 2019 911 GT3 models with child restraint system installation instructions that may not meet safety standards, requiring manual updates to prevent crash injuries.
PorscheNov 12, 2019 - Use cautionVehicle
POLARIS SLINGSHOT (2019) recall — Electrical System
Polaris recalls 2019 Slingshot models with defective 10A circuit breaker causing engine stalls. Owners must get free repair to prevent crashes.
PolarisNov 12, 2019 - Use cautionVehicle
INDIAN SPRINGFIELD DARK HORSE (2019) recall — Electrical System
Indian is recalling 2019 Dark Horse motorcycles due to a defective 10A circuit breaker that can cause sudden power loss and engine stalls, increasing crash risk. Owners will receive free installation of a new circuit breaker.
IndianNov 12, 2019 - Use cautionVehicle
FORD F-550 SD (2019) recall — Structure
Ford is recalling 2017-2019 F-550 SuperCrew Cab vehicles with carpet flooring due to fire risk if seat belt pretensioner sparks ignite materials. Owners must have heat-resistant tape applied to prevent fire.
FordNov 12, 2019 - Use cautionVehicle
TRIPLE E UNITY (2020) recall — Equipment
Triple E is recalling 2020 Unity U24RL trailers where propane tubing near tires could cause leaks and fire if damaged by tires.
Triple ENov 12, 2019 - Use cautionVehicle
TOYOTA COROLLA (2020) recall — Seat Belts
Toyota is recalling 2020 Corollas with rear seat belts that may not lock properly during crashes, increasing injury risk. Owners must contact Toyota for free replacement.
ToyotaNov 12, 2019 - Use cautionVehicle
PORSCHE 911 CARRERA (2020) recall — Exterior Lighting
Porsche is recalling certain 2020 911 Carrera models due to hazard warning lights not functioning properly, which could increase crash risk in hazardous conditions. Owners must contact Porsche for free reprogramming.
PorscheNov 12, 2019 - Use cautionVehicle
BMW M5 (2020) recall — Power Train
BMW recalls 2019-2020 M5 and M8 models for potential transmission short circuits causing loss of propulsion and crash risk. Free repairs to be done by dealers starting February 3, 2020.
BMWNov 12, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls ApexPro Telemetry System - Product Usage: The ApexPro Telemetry System is intended for use under the direct supervision
GE Healthcare recalls specific ApexPro Telemetry System units for cybersecurity vulnerabilities that could allow unauthorized network access when connected to hospital networks. Affected units have unique serial numbers listed in the recall notice.
GE HealthcareNov 12, 2019 - Lower riskMedical device
Aesculap Implant Systems LLC recalls ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during
Aesculap recalls Enduro Special Key Tib Lock Ring F1/10mm (product code NP462R) used in knee surgery due to potential key pin damage during assembly. Affected items sold with EnduRo Total Knee System.
AesculapNov 12, 2019 - UnratedDrug
Integrated Health Concepts Inc. dba Conversio Health recalls Albuterol 2.5mg / Ipratropium 0.75mg/ Triamcinolone 0.5 mg 3ML Vial, For Inhalation Only, Conversio Health, San Luis
Conversio Health recalls albuterol inhaler vials due to lack of processing controls. All lots affected. No specific remedy stated in official notice.
Conversio HealthNov 12, 2019 - Lower riskDrug
AuroMedics Pharma LLC recalls Fluphenazine Decanoate Injection USP 125mg/5mL, (5 mL Multiple Dose Vial), Rx only, For IM or SC Use, Mfd in India for:
AuroMedics Pharma recalls Fluphenazine Decanoate Injection vials with discoloration or hazy solution. This may affect patients using injectable medication for mental health conditions.
AuroMedicsNov 12, 2019 - Stop using nowDrug
QuVa Pharma, Inc. recalls fentaNYL 2000 mcg/100 mL (20 mcg/mL) in 0.9% Sodium Chloride, 100 mL Bag, Preservative Free, Rx, QuVA Pharma 1075 West
QuVa Pharma recalls fentanyl 2000 mcg/100mL bags due to potential glass particles. Affected lots expire through January 2020. Consumers should check product details and contact manufacturer for guidance.
QuVa PharmaNov 12, 2019 - Lower riskFood
SIMPLOT-RDO LLC recalls Simplot simple goodness Classic Mixed Vegetables, foodservice item. There are 12/2.5 lbs. clear plastic bags per case.
Simplot recalls foodservice mixed vegetables due to undeclared soy (edamame) in the product. Consumers should check labels for soy ingredients and contact Simplot for details.
SimplotNov 12, 2019 - Stop using nowFood
AC Culinary Group LLC. recalls Chef Pineiro's Ajo con Cilantro, with Coriander, NET WT./PESO NETO 8 oz (233g) and NET WT./PESO NETO 32 oz (907g)
Chef Pineiro's Ajo con Cilantro (8oz & 32oz) with metal filament in bottles. Recalled lots #8,9,14,15,21 exp 10/2020. Stop using to avoid injury.
Chef Pineiro'sNov 12, 2019 - Use cautionConsumer product
Hooey Recalls Children's Sweatshirts with Drawstrings Due to Strangulation Hazard
Hooey recalls 15 youth sweatshirt styles with drawstrings that can entangle on playground equipment, posing strangulation risk to children. Remove drawstring immediately to eliminate hazard.
HooeyNov 12, 2019 - Lower riskMedical device
Abbott Medical recalls CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable
Abbott Medical recalls a specific lot of Classic Radiofrequency Cannulas due to incorrect tip length labeling, which may lead to improper lesion size during medical procedures.
Abbott MedicalNov 11, 2019 - Use cautionMedical device
Smith & Nephew, Inc. recalls smith&nephew PROFIX Mallet, 750 GRAMS, REF 71512452 - Product Usage: The PROFIX Mallet is a reusable surgical
Smith & Nephew recalls PROFIX Mallet surgical instruments with potential for poly tip to become loose during knee or hip surgery, risking particles entering the surgical field or delays.
Smith & NephewNov 11, 2019 - Lower riskMedical device
Nextremity Solutions recalls Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST
Nextremity Solutions recalls Stratum MDS Screw 3.5x50mm ST (part number STRM-MDS-3550ST) due to components being 2mm shorter than labeled. Affected units include lot M1268 with UDI 00817701023173.
Nextremity SolutionsNov 11, 2019 - Lower riskMedical device
Medicrea International recalls Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500
Medicrea International recalls Universal Counter Torque (A22020500) due to incompatibility with Pass TULIP [Spinal] System nut drivers. Affected units may cause improper installation.
Medicrea InternationalNov 11, 2019 - Lower riskDrug
AuroMedics Pharma LLC recalls Lidocaine HCl Injection, USP, 2% 100 mg/5 mL (20 mg/mL), Preservative-Free, packaged in 10 x 5 mL Single Dose Vials per
AuroMedics Pharma recalls 2% Lidocaine HCl injection vials due to foreign material found inside. This product is prescription-only and may pose a risk if used without proper cleaning.
AuroMedicsNov 11, 2019
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.