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 cautionMedical device
Skytron, Div. The KMW Group, Inc recalls Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part
Skytron recalls Ergon 3 Series Skyboom Monitor Brackets with potential weld failure at pivot point, risking display falls and injury. Affected units have specific serial numbers.
SkytronMar 5, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Epinephrine Injection USP, 0.3 mg (Auto-Injector), 0.3 mg/ 0.3 mL pre-filled syringe, Rx Only, Manufactured for Teva
Teva recalls Epinephrine Injection USP 0.3 mg auto-injectors due to out-of-specification trigger force in a non-marketed lot. This may affect safety during use.
TevaMar 5, 2020 - UnratedDrug
Fresenius Medical Care Holdings, Inc. recalls Sodium Chloride 0.9% Injection, USP, 1000 mL bags, Rx only, Manufactured by: Fresenius Medical Care North America,
Fresenius Medical Care recalls 1000mL Sodium Chloride 0.9% Injection bags with improper sterilization indicators. This may affect safety during medical use. Contact for details.
Fresenius Medical CareMar 5, 2020 - Lower riskFood
Stonewall Kitchen, LLC recalls Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato
Stonewall Kitchen recalls 16oz Ghost Pepper Salsa due to mislabeling as salsa but containing queso and failing to declare milk and soy allergens. Consumers should check product labels for the specific UPC and best by date.
Stonewall KitchenMar 5, 2020 - Stop using nowConsumer product
RH Recalls Floor Lamps Due to Fire Hazard (Recall Alert)
RH recalls Camino floor lamps due to fire risk from overheating on/off switch. Stop using and get a refund.
RHMar 5, 2020 - Stop using nowConsumer product
Joules USA Recalls Children's Pajamas and Robes Due to Violation of Federal Flammability Standard; Burn Hazard
Joules recalls children's pajamas and robes that fail federal flammability standards, risking burns. Consumers must stop using and return for refund.
JoulesMar 5, 2020 - Stop using nowConsumer product
ECHO Recalls Backpack Blowers and Replacement Shoulder Straps Due to Laceration and Impact Hazards
ECHO recalls 2-cycle gas backpack blowers with shoulder straps that can expel plastic pieces causing lacerations or impacts. Return to authorized dealer for free repair.
ECHOMar 5, 2020 - Stop using nowVehicle
ISUZU NPR (2019) recall — Service Brakes
Isuzu recalls certain 2019 NPR and Chevrolet 4500 vehicles due to rear brake line clips potentially failing, which could cause reduced braking.
IsuzuMar 4, 2020 - Use cautionVehicle
ISUZU FTR (2020) recall — Electrical System
Isuzu recalls certain 2018-2020 FTR vehicles due to electrical harness routing that may cause stalling or ABS failure, increasing crash risk. Owners must have wire harness repaired or replaced by dealers.
IsuzuMar 4, 2020 - Use cautionVehicle
FORD RANGER (2020) recall — Power Train
Ford recalls 2020 Ranger vehicles with 10-speed automatic transmissions for potential unintended movement if parking brake isn't applied. Owners must have shift cable inspected by dealers.
FordMar 4, 2020 - Lower riskMedical device
Diagnostica Stago, Inc. recalls STA - Deficient VIII, Product Code: 00725. STA - Deficient VIII is an immuno-depleted human plasma intended for use in
Stago recalls STA Deficient VIII product code 00725 due to risk of false high factor VIII results from cross-contamination. Affected units include specific STA-R and STA Compact analyzers with listed product codes and software versions.
StagoMar 4, 2020 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,
RaySearch Laboratories recalls RayStation software versions 4.0-9.1 due to potential inaccuracies in radiation treatment planning that could lead to uneven dose distribution in complex treatments.
RaySearchMar 4, 2020 - Lower riskDrug
Par Pharmaceutical Inc. recalls PrediniSONE Tablets, USP 5 mg, 48-count bottle, Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977,
Par Pharmaceutical recalls Prednisone 5mg tablets with incorrect expiration dates. Consumers should check labels for exp date and contact the company for details.
Par PharmaceuticalMar 4, 2020 - Use cautionConsumer product
IKEA Recalls KULLEN 3-Drawer Chests Due to Tip-Over and Entrapment Hazards; Consumers Urged to Anchor Chests or Return for Refund
IKEA recalls KULLEN 3-drawer chests not anchored to wall due to tip-over and entrapment hazards. Consumers must anchor or return for refund to prevent serious injury risks to children.
IKEAMar 4, 2020 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Seats
Blue Bird is recalling certain 2019 All American school buses with improperly installed seat barriers that may not protect occupants in crashes. Owners must have the seat barrier inspected and reinforced by dealers by April 23, 2020.
Blue BirdMar 3, 2020 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Service Brakes, Air
Daimler Trucks North America recalls 2020 Thomas Built Saf-T-Liner C2 school buses with air disc brakes due to loose brake caliper mounting bolts that may reduce brake effectiveness, increasing crash risk. Owners must contact DTNA for free repairs.
Thomas Built BusesMar 3, 2020 - Use cautionVehicle
JEEP GLADIATOR (2020) recall — Power Train
Chrysler recalls 2020 Jeep Gladiator vehicles with manual transmissions due to overheated clutch components that could cause fire or crash risks. Owners must contact customer service for repairs.
ChryslerMar 3, 2020 - Use cautionVehicle
FCCC XCR (2020) recall — Service Brakes, Air
Daimler Trucks North America recalls 2019-2020 Freightliner models with air disc brakes due to loose brake caliper bolts that could reduce brake effectiveness and increase crash risk. Free repair available.
DTNAMar 3, 2020 - Use cautionMedical device
Canon Medical System, USA, INC. recalls Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital
Canon recalls Infinix-8000F systems with CAT-850B or CAT-860B catheterization tables due to loose bolts causing table tilting. Affected units have specific serial numbers listed in the recall notice.
Canon MedicalMar 3, 2020 - Use cautionMedical device
Capintec Inc recalls Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by
Capintec recalls specific models of thyroid uptake systems due to potential collimator assembly falling and contacting patients or operators during use.
CapintecMar 3, 2020 - Stop using nowDrug
Yusef Manufacturing Laboratories, LLC recalls PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15, 4.2 g tube, labeled as a) Bimark Inc.,
Yusef Manufacturing Laboratories recalls PEPPERMINT LIP MOISTURIZER with high oxybenzone content (up to 150% of label) that may cause adverse reactions. Consumers should check product details and contact the manufacturer.
Yusef Manufacturing LaboratoriesMar 3, 2020 - Lower riskFood
Tops Markets Inc. recalls Tops Mint Flavor Pure Dark Chocolate 45% Cocoa NET WT 3.5 oz.(100g)
Tops Markets recalls mint dark chocolate bars with undeclared milk. Consumers should check best by dates and UPC codes for affected products.
Tops MarketsMar 3, 2020 - UnratedFood
Vita Food Products, Inc. recalls Vita Wild Herring in Wine Sauce 32oz plastic jar, UPC 22635 40011, 6 jars per case Ready to Eat Keep Refrigerated
Vita Food Products recalls 32oz plastic jars of Wild Herring in Wine Sauce due to undeclared milk. Products sold with UPC 22635 40011, 6 per case. Keep refrigerated until June 26, 2020.
VitaMar 3, 2020 - Lower riskMedical device
CSL Behring GmbH recalls Siemens N Latex CDT Kit- IVD quantitative determination of carbohydrate-deficient transferrin (CDT) in human serum.
Siemens N Latex CDT Kit may show inaccurate results after 15 months. Recalled due to negative bias in carbohydrate-deficient transferrin measurements compared to HPLC method. No remedy specified.
CSL BehringMar 2, 2020 - Use cautionMedical device
Merits Holdings Co. dba Merits Health Products, Inc. recalls Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.
Merits Health recalls E604 Pilot Navigator stairlifts due to pinion gear disengaging from track, risking slips or jolts during patient transport.
Merits HealthMar 2, 2020 - Lower riskDrug
Mayne Pharma Inc recalls Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC
Mayne Pharma recalls 100-count Carbidopa-Levodopa tablets (25mg/250mg) due to a foreign tablet found in the bottle. This Rx-only medication is for Parkinson's disease treatment.
Mayne PharmaMar 2, 2020 - Lower riskDrug
Noven Therapeutics, LLC recalls Daytrana (methylphenidate transdermal system) patches, Delivers 20 mg over 9 hours (2.2 mg/hr), 30-count box, Rx only,
Noven Therapeutics recalls Daytrana (methylphenidate transdermal patches) due to defective delivery system causing incorrect dosing. 30-count boxes with specific NDC numbers are affected.
Noven TherapeuticsMar 2, 2020 - Lower riskFood
Whole Foods Market recalls Whole Foods Market Green Chile Chicken Tamale served as a Family Meal, Chef's Case, Packaged, Frozen and on he hot bar
Whole Foods Market recalls Green Chile Chicken Tamales served as Family Meals due to undeclared milk content. Consumers should check product codes and dates for affected items.
Whole Foods MarketMar 2, 2020 - Stop using nowFood
New Capstone, Inc recalls ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G SINGLE PACKET Other Ingredients: Non-GMO rBGH-Free Whey
New Capstone, Inc. recalls ReStructure Vanilla Protein Powder because the label fails to declare milk, posing a risk to those with allergies.
ReStructureMar 2, 2020 - Lower riskFood
Global Juices & Fruits LLC recalls Nature's Earthly Choice Organic Lentil Trio product containing a blend of red split, black and green lentils, labeled
Nature's Earthly Choice Organic Lentil Trio (gluten-free) recalled due to gluten contamination. Some pouches contained barley, wheat, or other gluten-containing grains. Consumers should avoid use.
Nature's Earthly ChoiceMar 2, 2020
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