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
34,894 found- Use cautionMedical device
Arjohuntleigh Magog recalls Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to
Arjohuntleigh Magog recalls Q-Connect 272 KG Scales used with Maxi Sky 2 ceiling lifts due to spreader bar detachment risk. Affected units have serial numbers 300142013 to 300219867.
Arjohuntleigh MagogFeb 12, 2018 - Use cautionMedical device
Boston Scientific Corporation recalls Capio SLIM Box 5, Model #M0068318261; Intended for use in general suturing applications during open surgery to assist
Boston Scientific recalls Capio SLIM Box 5 sutures with model #M0068318261 due to potential breakage or detachment during open surgery, which could lead to complications.
Boston ScientificFeb 12, 2018 - Lower riskFood
Heartland Coca-Cola Bottling Company recalls Grape Fanta, Grape Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola
Heartland Coca-Cola recalls Grape Fanta 12-oz cans due to sharp edges that could cause mouth cuts. Consumers should check if their cans have the potential for cuts.
Heartland Coca-ColaFeb 12, 2018 - Use cautionVehicle
JAYCO PRECEPT (2019) recall — Wheels
Jayco is recalling 2019 Precept motorhomes with unheat-treated wheel studs that could break, risking vehicle crashes. Owners must have hubs inspected and studs replaced free by Ford dealers.
JaycoFeb 10, 2018 - Use cautionVehicle
ENTEGRA ANTHEM (2019) recall — Equipment
Entegra is recalling 2019 Anthem motorhomes with improperly adjusted door latch rods that may open during transit, increasing crash risk. Owners should contact Entegra for free door adjustment.
EntegraFeb 10, 2018 - Use cautionVehicle
ENTEGRA ANTHEM (2019) recall — Service Brakes, Air
Entegra is recalling 2019 Anthem motorhomes with faulty park brakes that may move unintentionally when parked on slopes, risking crashes. Owners must contact customer service for free brake repairs.
EntegraFeb 10, 2018 - Lower riskDrug
Apace KY LLC recalls Acyclovir Tablets, USP, 400 mg, 50 Tablets (5 x 10) unit dose blisters [NDC 50268-061-11] per carton [NDC
Apace KY recalls Acyclovir tablets that may contain Torsemide tablets in some blister cavities. This could cause unintended medication effects.
Apace KYFeb 9, 2018 - Lower riskDrug
American Pharmaceutical Ingredients LLC recalls Nifedipine USP for prescription compounding, packaged in a) 5g (NDC 58597-8025-2); b) 25g (NDC 58597-8025-4); c) 100g
American Pharmaceutical Ingredients LLC recalls specific Nifedipine USP batches due to lack of stability data affecting expiration dates. These are prescription-only compounds for medical use.
American Pharmaceutical IngredientsFeb 9, 2018 - Lower riskFood
InHarvest, Inc. recalls White Quinoa; 16 oz. (454g) bags with clear panel in front; UPC: 0 72431 00195 6 Brand name Lunds & Byerlys Quinoa
Lunds & Byerlys recalls 16oz White Quinoa bags with clear panel that may contain undeclared wheat. Consumers should check UPC 072431001956 for affected products.
Lunds & ByerlysFeb 9, 2018 - UnratedFood
Divinity Product Distribution LLC recalls Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,
Divinity Product Distribution LLC recalls Kratom capsules due to insufficient safety data for kratom. Consumers should check labels for specific product names and expiration dates after January 31, 2018.
DivinityFeb 9, 2018 - Use cautionVehicle
THOR MOTOR COACH VENETIAN (2019) recall — Service Brakes, Hydraulic
Thor Motor Coach is recalling 2019 Venetian motorhomes with potentially loose brake caliper mounting bolts that could reduce braking performance and increase crash risk. Owners should contact TMC for free inspection.
Thor Motor CoachFeb 8, 2018 - Use cautionVehicle
SUBARU ASCENT (2019) recall — Structure
Subaru is recalling certain 2019 Ascent vehicles that may have missing spot welds around the B-Pillar, which could weaken the vehicle's structure during a crash. Owners should contact Subaru for inspection and potential replacement.
SubaruFeb 8, 2018 - Use cautionVehicle
NEWMAR VENTANA (2019) recall — Service Brakes, Hydraulic
Newmar is recalling 2017-2019 Ventana motorhomes for potentially loose brake caliper mounting bolts that could reduce braking performance and increase crash risk. Affected owners should contact Newmar for free brake inspection.
NewmarFeb 8, 2018 - Stop using nowMedical device
Medtronic Perfusion Systems recalls BIO CAL(R) Temperature Controller, Models: (a) 370, (b) 370I Product Usage: The BIO CAL(R) (unit) is a thermal transfer
Medtronic recalls BIO CAL(R) Temperature Controllers (Models 370 and 370I) due to inability to develop a safe cleaning protocol. Affected units must be discontinued and disposed of immediately.
Medtronic Perfusion SystemsFeb 8, 2018 - Lower riskMedical device
Life Technologies Corporation recalls Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In
Life Technologies recalls two cancer test kits due to potential false negatives in ROS1 fusion detection, which could lead to incorrect treatment decisions.
Life TechnologiesFeb 8, 2018 - Use cautionMedical device
Stanbio Laboratory, LP recalls Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series. The firm name on the label for the HemoPoint
Stanbio recalls AC power adapters for HemoPoint H2 meters (Model G3000) due to risk of electrical exposure from cracked plugs. Affected units have serial numbers 41800001-41804000.
StanbioFeb 8, 2018 - Use cautionMedical device
Bovie Medical Corporation recalls J-Plasma Precise 360(R), Catalog Numbers: BVX-330BR, BVX-330NR, BVX-450BR, BVX-450NR
Bovie Medical recalls J-Plasma Precise 360(R) devices with specific catalog numbers and production dates due to risk of patient fluid backflow and cross-contamination if the generator is reused.
Bovie MedicalFeb 8, 2018 - Lower riskMedical device
Tornier, Inc recalls Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM PHANTOM FT BIOCOMPOSITE SUTURE ANCHOR WITH
Tornier recalls Phantom Fiber sutures that may lose strength faster if improperly stored, potentially affecting surgical safety. Affected items include specific sizes and packaging. Consumers should check product details and contact Tornier for guidance.
TornierFeb 8, 2018 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362
Bard recalls POWERPORT ClearVUE implantable ports with incorrect flushing instructions that could lead to improper use. Affected units have specific lot numbers and reference codes.
BardFeb 8, 2018 - Use cautionMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance Big Bore (Radiology) - Model no. 728244, Computed Tomography X-Ray system Product Usage: Computed Tomography
Philips recalls specific models of Brilliance Big Bore CT scanners due to risk of couch movement during patient loading/unloading if Emergency Stop is closed. Affected units have serial numbers listed in the recall notice.
Philips Medical SystemsFeb 8, 2018 - Lower riskFood
Vitalab Co Inc recalls Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet
Vitalab recalls Vitamin C supplements containing lactose that fail to list milk as a major allergen on labels. This affects specific lots sold through Sonne's and Springreen. Consumers should check labels for the listed lot numbers.
VitalabFeb 8, 2018 - Lower riskFood
WEIS MARKETS recalls Weis Sunbury, PA 17801; Penne W/Asiago Sauce And Grilled Chix Small Meal; multiple weight. SCALE UPC - 205377-00000
Weis Markets recalls Penne W/Asiago Sauce and Grilled Chix Small Meal due to undeclared milk. Consumers should check product UPC 205377-00000 for affected items.
Weis MarketsFeb 8, 2018 - Stop using nowConsumer product
Poppin Recalls Pitch Rolling Chairs Due to Fall Hazard (Recall Alert)
Poppin recalls five-color pitch rolling chairs due to seat plate detachment causing fall hazards. Affected models include Red (103772), Blue (103767), Dark Gray (103769), Khaki (103771), and Dark Blue (103768).
PoppinFeb 8, 2018 - Stop using nowConsumer product
Husqvarna Recalls Residential Zero Turn Riding Mowers Due to Fire Hazard
Husqvarna recalls residential zero turn riding mowers with Briggs & Stratton engines due to fire risk from fuel line leaks. Consumers must stop using and get repairs.
HusqvarnaFeb 8, 2018 - Stop using nowConsumer product
Fujitsu Recalls Battery Packs for Fujitsu Notebook Computers and Workstations Due to Fire and Burn Hazards
Fujitsu recalls Panasonic lithium-ion battery packs for notebook computers and workstations due to fire and burn risks. Affected models include CELSIUS H720 and LIFEBOOK E752 series. Consumers must stop using and replace immediately.
FujitsuFeb 8, 2018 - Lower riskMedical device
Life Technologies Corporation recalls Human Fetal Hemoglobin (HBF-1) FITC Conjugate
Life Technologies recalls three lots of Human Fetal Hemoglobin FITC Conjugate due to potential false positives in tests. Affected units may cause incorrect results in patient samples and controls.
Life TechnologiesFeb 7, 2018 - Lower riskMedical device
Advanced Instruments, LLC recalls GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Counter System is intended for use by trained
Advanced Instruments recalls GloCyte RBC Reagent due to high fluorescent counts causing failed QC checks, preventing accurate patient sample testing in clinical labs.
Advanced InstrumentsFeb 7, 2018 - Lower riskMedical device
Philips Electronics North America Corporation recalls HeartStart XL+ Defibrillator/Monitor The HeartStart XL+ is intended for use in a hospital setting by qualified medical
Philips recalls HeartStart XL+ Defibrillators made before Sept 2017 that need software update A.03 for operational safety. Update to prevent incomplete device readiness checks.
PhilipsFeb 7, 2018 - Lower riskMedical device
Medela Inc recalls Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model
Medela recalls Invia Motion Negative Pressure Wound Therapy systems with battery missing error display. Affected models include Endure (087.4010) and 15/60-day therapy versions. No remedy specified in recall notice.
MedelaFeb 7, 2018 - Use cautionMedical device
GETINGE US SALES LLC recalls VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901,
GETINGE recalls VOLISTA StandOP Surgical Lights with model numbers VLT600 SF AIM STP and VLT600 DF AIM STP due to handle holder detaching during use, risking particles falling into the sterile surgical field.
GETINGEFeb 7, 2018
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