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
34,896 found- Lower riskMedical device
Beckman Coulter Inc. recalls iChem VELOCITY Automated Urine Chemistry System, Catalog #700-7176-001 and iChem VELOCITY Automated Urine Chemistry
Beckman Coulter recalls iChem VELOCITY Automated Urine Chemistry Systems with defective seal placement in Strip Provider Modules. Affected units may have manufacturing flaws that could lead to inaccurate test results.
Beckman CoulterMar 29, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP) Catheter, catalog numbers D135303 and D135304.
Stryker Sustainability Solutions recalls two specific Coronary Sinus Uni-Directional Diagnostic EP Catheter models (D135303/D135304) due to failing non-thrombogenic specifications in testing. The catheters are used for cardiac electrophysiology mapping.
Stryker Sustainability SolutionsMar 29, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is
Zimmer Biomet recalls specific segmental system proximal femoral components for possible debris in the hole during machining, which may not have been fully cleaned. This affects certain surgical implants used in complex bone repair cases.
Zimmer BiometMar 29, 2018 - Use cautionMedical device
Cook Inc. recalls Connecting Tube - Female to Male Luer Lock, HPCT8.8-60-M-FM-BNS Product Usage: The connecting tube is intended to be a
Cook recalls HPCT8.8-60-M-FM-BNS connecting tubes for potential fluid leakage during angiography procedures. Affected units may cause air aspiration or fluid leakage if the cap-adapter assembly isn't properly tightened.
CookMar 29, 2018 - Use cautionMedical device
GE Medical Systems, SCS recalls Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems
GE Medical Systems recalls Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems due to potential X-ray abort errors causing imaging loss during procedures. Affected units have specific model and lot numbers.
GE Medical SystemsMar 29, 2018 - UnratedDrug
United Pacific Co Ltd recalls Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02
United Pacific recalls Zhong Hua Jiu menthol 1% patches due to substandard manufacturing processes. Affected lots have specific expiration dates and UPC/NDC codes.
United PacificMar 29, 2018 - Lower riskDrug
Akorn, Inc. recalls 24-HOUR Oral Care q2 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine
Akorn recalls 24-Hour Oral Care q2 Kit with Ballard Technology containing chlorhexidine that may have low drug potency due to crystallization. This could affect treatment effectiveness. Consumers should contact Akorn for details.
AkornMar 29, 2018 - Lower riskFood
R.A.B. Food Group LLC recalls Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized bag in gable box,
Manischewitz recalls Dark Chocolate Potato Chips due to undeclared peanuts, tree nuts, and milk. Consumers should check for lot #1J026 and avoid if allergic.
ManischewitzMar 29, 2018 - Use cautionFood
purely elizabeth. recalls Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,
Purely Elizabeth recalls 8oz Chocolate Sea Salt Probiotic Granola pouches due to undeclared soy lecithin. Check your pantry for affected lots.
Purely ElizabethMar 29, 2018 - Lower riskFood
Health Nuts recalls Healthy Nut Factory ORGANIC COCONUT SMILES, Net Wt. 7 oz, UPC: 8 13449 02099 3
Health Nuts recalls Organic Coconut Smiles (7 oz) due to possible Salmonella contamination. Consumers should check UPC 8 13449 02099 3 and discard if expired by 6/1/2018.
Health NutsMar 29, 2018 - Stop using nowConsumer product
Residential Elevators Recalls to Inspect Elevators Due to Impact Hazard (Recall Alert)
Recalled traction elevators (models LLT-952-955) installed 2015-2017 may stop unexpectedly, causing impact injuries. Contact for free inspection or repair.
Residential ElevatorsMar 29, 2018 - Use cautionConsumer product
Primo Recalls Beverage Dispensers Due to Burn Hazard
Primo hTrio multi-purpose beverage dispensers sold by Dec 31, 2017 may cause burns if used above 6,000 feet elevation. Consumers in high-altitude areas should stop using and get a free replacement.
PrimoMar 29, 2018 - Stop using nowConsumer product
Octane Fitness Recalls Cross Trainers Due to Fall Hazard (Recall Alert)
Octane Fitness recalls XT5700 cross trainers due to a fall hazard. The incline lead screw can shear, causing pedals to drop unexpectedly. Stop using immediately.
Octane FitnessMar 29, 2018 - Stop using nowConsumer product
H-E-B Recalls Halogen Lightbulbs Due to Laceration and Fire Hazards
H-E-B recalls GTC halogen light bulbs that can shatter in use, causing lacerations and fire hazards. Consumers should stop using and return for refund.
GTCMar 29, 2018 - Stop using nowMeat & poultry
Tony Downs Food Company, Inc. Recalls Chicken Products due to Possible Foreign Matter Contamination
USDA FSIS recalls 96,384 pounds of chicken products from Tony Downs Food Company due to possible hard plastic contamination. Consumers are urged not to consume these products.
Tony Downs Food CompanyMar 28, 2018 - Use cautionVehicle
TOYOTA CAMRY (2018) recall — Engine And Engine Cooling
Toyota is recalling 2018 Camry vehicles with a 2.5L engine that may stall, increasing crash risk. Affected vehicles need free piston replacement by dealers starting May 25, 2018.
ToyotaMar 28, 2018 - Use cautionVehicle
LOOK CARGO TRAILER (2018) recall — Suspension
LGS is recalling 2018 Look, Pace, and Cargo Express cargo trailers due to spindle weld failure that could cause loss of vehicle control and crashes.
LGSMar 28, 2018 - Use cautionVehicle
FLEETWOOD PACE ARROW (2018) recall — Equipment
REV is recalling 2018 Fleetwood Pace Arrow motorhomes due to satellite dish detachment risk while driving, which could cause crashes or injuries. Owners must have the dish resecured by dealers free of charge.
REVMar 28, 2018 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a
RaySearch Laboratories recalls RayStation versions 6.0-7.0 due to potential dose calculation errors in radiation therapy planning. Users must verify calculations to avoid incorrect treatments.
RaySearch LaboratoriesMar 28, 2018 - Lower riskMedical device
Ace Surgical Supply Co., Inc. recalls Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 Used to achieve epithelial graft in the oral cavity.
Ace Surgical Supply recalls Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 due to incorrect packaging. A single blade shoe was mistakenly included instead of a double blade.
Ace Surgical SupplyMar 28, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Gentle Threads, Interference Screw; Model No. 905604, for soft tissue reattachment procedures in the ankle/foot and
Zimmer Biomet recalls specific lots of Gentle Threads Interference Screw (Model 905604) due to potential infection from overexposure during EtO sterilization.
Zimmer BiometMar 28, 2018 - Lower riskMedical device
Cardinal Health 200, LLC recalls Medi-Vac(TM) Flex Advantage(TM) Suction Canister Liner, Material Numbers: a) REF 6561-910C b) REF 6561-916K c) REF
Cardinal Health recalls Medi-Vac Flex Advantage Suction Canister Liners with missing one-way valves that could cause fluid leaks during medical procedures. Affected models include REF 6561-910C and REF 6561-916K.
Cardinal HealthMar 28, 2018 - Lower riskMedical device
Draegar Medical Systems, Inc. recalls Infinity Acute Care System (lACS) Monitoring Solution; Catalog Numbers:MS20401, MS20724, MS22956, MS25510, MS25520,
Draegar Medical recalls Infinity Acute Care System monitoring devices due to software anomaly that may cause loss of patient settings and stored medical data. Affected models include MS20401, MS20724, etc.
Draegar MedicalMar 28, 2018 - UnratedMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance Big Bore Radiology 728244
Philips recalls specific Brilliance Big Bore Radiology 728244 models due to potential oil leakage from X-ray tube housing, which could pose risks during use. Affected units have unique serial numbers and UDI codes.
Philips Medical SystemsMar 28, 2018 - UnratedDrug
Elroselabs Inc. recalls Conzerol zero molluscum contagiosum, Topical Cream, Net weight 0.78 (22g), Elrose Labs, Sanford Fl 32771 USA --- NDC
Elrose Labs recalls Conzerol Zero topical cream due to cGMP deviations. Affected units have NDC 70223-001-06. No specific remedy stated in official notice.
Elrose LabsMar 28, 2018 - Lower riskFood
Independent Nutrition, Inc. recalls Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2.
Back to Health Ignite High Endurance Pre-Workout Supplement with Caffeine is recalled because it claims to contain whey protein but does not list milk as an ingredient. This may cause allergic reactions in people with milk allergies.
Back to HealthMar 28, 2018 - Stop using nowConsumer product
Shop LC Recalls Electric Blankets Due to Fire and Burn Hazards (Recall Alert)
Shop LC recalls electric heated micro plush flannel sherpa throw blankets due to fire and burn hazards from overheating heating coils. Affected units have date code 22217 and model OB205B2.
Shop LCMar 28, 2018 - Use cautionVehicle
NEWMAR VENTANA (2017) recall — Steering
Newmar recalls 2014-2017 Ventana models with faulty power steering hose that may leak fluid or cause electrical arcing, risking fire or crash. Owners must have hose rerouted by dealers.
NewmarMar 27, 2018 - Use cautionMedical device
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in
Teleflex Medical recalls Hudson RCI One Way Valve (REF 1644) due to potential disconnection causing ventilation interruption. Affected units sold in respiratory/anesthesia circuits.
Teleflex MedicalMar 27, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use on ADVIA 1800, 2400 and XPT Chemistry Systems
Siemens Healthcare recalls ADVIA Urea Nitrogen reagent kits for ADVIA 1800/2400/XPT systems due to calibration failures preventing test results.
Siemens HealthcareMar 27, 2018
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83,392 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.