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- Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayPlan 1 (RayStation 4.9)
RaySearch Laboratories recalls specific RayStation software versions due to potential dose calculation errors in radiation therapy planning. Affected versions include 3.5 through 6.2.
RaySearch LaboratoriesNov 20, 2017 - Lower riskDrug
Teva Pharmaceuticals USA recalls Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP, 90mcg/20mcg), 28 tablet dispenser (blister foil unit), Rx
Teva recalls Amethyst birth control pills due to incorrect labeling that says some tablets are inactive when all are active. This could lead to unintended pregnancy if users skip doses.
Teva Pharmaceuticals USANov 20, 2017 - Lower riskDrug
Zydus Pharmaceuticals USA Inc recalls Paroxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-099-05), and c) 1000 count (NDC
Zydus Pharmaceuticals USA recalls 30mg Paroxetine tablets due to presence of Risperidone tablets in some bottles. This could cause unintended medication intake. Return or contact for remedy.
Zydus PharmaceuticalsNov 20, 2017 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Glenmark Mometasone Furoate Cream, USP, 0.1%, 45 g Rx Only Manufactured by: Glenmark Pharmaceuticals Ltd. Village
Glenmark Pharmaceuticals recalls 0.1% Mometasone Furoate Cream due to gritty texture complaints. This Rx-only cream may cause irritation. Check NDC 68462019255 for affected batches.
GlenmarkNov 20, 2017 - Lower riskFood
Clover Hill Dairy recalls Clover Hill Dairy, Soft Ricotta
Clover Hill Dairy is recalling Soft Ricotta due to potential contamination from improper silo cleaning during production. Affected lots include B11 1317, C11 1317, B11 1517, and C11 1517. Consumers should check labels and contact the company for details.
Clover Hill DairyNov 20, 2017 - Stop using nowDrug
www.blankterrmall.com recalls Hard Times For Men capsules, packaged in a 23-count box of blister packs containing one capsule per pack,
Hard Times For Men capsules (23-count blister packs) contain undeclared sildenafil, a prescription drug. Consumers should stop using these products immediately due to potential health risks.
Hard Times For MenNov 19, 2017 - Lower riskFood
Farrell Farms, Inc recalls Dark Chocolate Pecans Net Wt. 7 oz, Farrell Farms, 200 Gin Road, Goldsboro, NC
Farrell Farms recalls 7 oz Dark Chocolate Pecans sold online from Oct 16-17, 2017 due to undeclared milk allergen. Consumers should check product labels for milk content.
Farrell FarmsNov 19, 2017 - Stop using nowMeat & poultry
Green Cuisine Recalls Poultry Products Due To Possible Foreign Matter Contamination
Green Cuisine recalls 65,621 pounds of chicken and turkey salads from Nov. 4-15, 2017, potentially contaminated with glass and silica fragments. Consumers urged not to eat these products.
Green CuisineNov 18, 2017 - Use cautionVehicle
HOLIDAY RAMBLER AMBASSADOR (2013) recall — Equipment
REV recalls 2013 Holiday Rambler Ambassador motorhomes with Kidde fire extinguishers that may become clogged or detach, increasing injury risk during fires. Owners must contact REV or Kidde for a free replacement.
REVNov 17, 2017 - Use cautionVehicle
NEWMAR LONDON AIRE (2017) recall — Exterior Lighting
Newmar is recalling 2015-2018 London Aire motorhomes with exterior lighting issues that may reduce driver visibility, increasing crash risk. Owners must contact Newmar for free repairs.
NewmarNov 17, 2017 - Use cautionVehicle
HONDA ODYSSEY (2017) recall — Seats
Honda is recalling certain 2011-2017 Odyssey vehicles due to second row seats that may slide and tip forward during braking, increasing injury risk. Owners will receive free bracket installation.
HondaNov 17, 2017 - Stop using nowVehicle
FOREST RIVER DYNAMAX (2017) recall — Engine And Engine Cooling
Forest River recalls certain 2017-2018 Dynamax RVs due to carbon monoxide entering the cabin. Dealers will install exhaust tips for free.
DynamaxNov 17, 2017 - Use cautionVehicle
FREIGHTLINER CASCADIA (2018) recall — Power Train
Daimler Trucks North America recalls 2018 Freightliner Cascadia trucks with Detroit automatic transmissions. A shift lock bolt can seize, causing engine stalls and crash risks. Owners must have transmission inspected and repaired free.
Daimler Trucks North AmericaNov 17, 2017 - Use cautionVehicle
BMW X5 (2018) recall — Suspension
BMW is recalling 2018 X5 models with potentially loose front suspension bolts that could increase crash risk. Owners must have suspension bolts inspected and tightened by dealers free of charge starting January 8, 2018.
BMWNov 17, 2017 - Use cautionMedical device
Ion Beam Applications S.A. recalls Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam for the treatment of
Ion Beam Applications recalls Proteus 235 proton therapy systems due to potential patient misalignment during multi-isocenter treatments. This medical device is used for cancer treatment. Affected units may require correction to ensure safe radiation delivery.
Ion Beam ApplicationsNov 17, 2017 - Lower riskMedical device
Edan Diagnostics recalls EDAN Telemetry Transmitter, Model iT20 - Product Usage: The iT20 telemetry transmitter is intended to be used in
Edan Diagnostics recalls 7 hospital telemetry transmitters (model iT20) sold in the U.S. with an unapproved FDA function. Affected units have specific serial numbers listed. No action is required as the issue is non-functional and not a safety hazard.
Edan DiagnosticsNov 17, 2017 - Lower riskMedical device
Cypress Medical Products LLC recalls 241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal
Cypress Medical Products recalls 241-McKesson Premium Skin Staple Remover Kit and related items due to iodine assay levels not meeting 36-month expiration requirements. Consumers should contact the manufacturer for details.
Cypress Medical ProductsNov 17, 2017 - Lower riskMedical device
Z-Medica, LLC recalls QuikClot TraumaPad, Part# 460 a topical dressing for local management of bleeding wounds such as cuts, lacerations, and
Z-Medica recalls QuikClot TraumaPad Part# 460 due to one pouch in a box containing the wrong type. All other pouches and packaging are correct. No action needed as the hazard is a labeling error, not a safety risk.
Z-MedicaNov 17, 2017 - Stop using nowMedical device
Accuray Incorporated recalls TomoHDA(R) System, Model Number 1018286 Product Usage: The TomoTherapy treatment system is intended to be used as an
Accuray recalls TomoHDA System model 1018286 due to uncontrolled couch descent during radiation therapy. Affected units have specific serial numbers; stop using immediately to prevent injury.
AccurayNov 17, 2017 - Lower riskMedical device
PerkinElmer Life and Analytical Sciences, Wallac, OY recalls Specimen Gate Screening Center, Part Number 5002-0500, All software versions from 1.0 to 1.8 (current software version)
PerkinElmer recalls Screening Center software versions 1.0-1.8 for potential false negative and positive patient results in newborn screening tests.
PerkinElmerNov 17, 2017 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA
CareFusion recalls Alaris PCA Pump Model 8120 due to risk of syringe plunger grippers failing to close properly, potentially causing medication delivery issues.
CareFusionNov 17, 2017 - Use cautionMedical device
Philips Electronics North America Corporation recalls IntelliVue X3 Patient Monitor.
Philips recalls IntelliVue X3 Patient Monitors with serial numbers DE61102743 to DE61101500 (shipped June 2017) due to inaccurate blood pressure readings and touchscreen issues.
PhilipsNov 17, 2017 - Lower riskMedical device
Stryker Corporation recalls STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 0234010056, labeled sterile.
Stryker recalls certain ACL Interface Screws (Model 0234010056) due to higher bioburden levels in some lots. Affected items may pose infection risks during surgery.
StrykerNov 17, 2017 - Lower riskDrug
Lupin Limited recalls Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,
Lupin Limited recalls 40mg Pravastatin tablets due to foreign tablets found in one bottle. This is a pharmacy complaint about a Duloxetine capsule being in the product.
Lupin LimitedNov 17, 2017 - Stop using nowFood
Plow And Hearth recalls 89291 Cashew Tower (Plow and Hearth Chocolate Covered Cashews). Net weight: 10 ounces . The product is package as a
Plow And Hearth is recalling 10-oz Cashew Tower chocolate-covered cashews that contain salted peanuts instead of cashews, posing an undeclared allergen risk.
Plow And HearthNov 17, 2017 - Lower riskFood
Virginia Diner Inc recalls Plow & Hearth Chocolate Covered Cashews
Virginia Diner Inc recalls Plow & Hearth Chocolate Covered Cashews due to undeclared peanuts. Consumers should check UPC 08558209193 for affected products.
Plow & HearthNov 17, 2017 - Lower riskFood
Elevation Brands, LLC recalls Ian's Gluten Free Original Panko Breadcrumbs, UPC# 7-49512-77550-0
Elevation Brands recalls Ian's Gluten Free Original Panko Breadcrumbs (UPC 7-49512-77550-0) due to potential beetle exposure from a raw material supplier. No insects found in finished products.
Ian's Gluten FreeNov 17, 2017 - Lower riskFood
Pure Encapsulations, Inc. recalls Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEMENT 180 CAPSULES UPC: 7 66298 00862 2
Pure Encapsulations recalls 180-capsule enzyme supplement due to undeclared sulfites. Affected lots include 50074561 through 50129551. Consumers should check their product and contact the company for details.
Pure EncapsulationsNov 17, 2017 - Use cautionConsumer product
Sleep Number Recalls Foot Warmers Sold with Sleep Number 360 Smart Beds Due to Burn Hazard (Recall Alert)
Recall for Sleep Number 360 smart bed foot warmers that can overheat and cause burns. Affected models sold from November 2016 include TwinXL, Full, Queen, King and other sizes with FlexFit 3 bases.
Sleep NumberNov 17, 2017 - Lower riskMeat & poultry
Trafon Group Recalls Chicken and Pork Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 297,828 pounds of chicken and pork products produced without U.S. import inspection. Consumers urged not to consume or discard items.
Trafon GroupNov 16, 2017
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,390 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.