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
34,893 found- Use cautionVehicle
CROSSROADS REDWOOD (2018) recall — Equipment
Keystone is recalling 2018 Crossroads Redwood trailers due to propane line damage risk of fire. Owners must contact customer service for free repairs to prevent leaks.
KeystoneAug 14, 2017 - Lower riskMedical device
Smiths Medical ASD Inc. recalls UniPerc(R) Adjustable Flange Tracheostomy Tube kit, Reorder Number 100/897/080 CZ The UniPerc(R) Tracheostomy Tubes can
Smiths Medical recalls UniPerc Adjustable Flange Tracheostomy Tube kits with incorrect 9.0mm obturator (lot 3308971). This could cause improper tube fitting during medical procedures.
Smiths MedicalAug 14, 2017 - UnratedMedical device
Edap Technomed Inc. recalls Ablatherm(R) Integrated Imaging, High Intensity Ultrasound System For Prostate Tissue Ablation Transrectal high
Edap Technomed recalls Ablather: Integrated Imaging ultrasound devices in the US for prostate ablation. FDA requires removal of medium and low energy settings until clinical data is submitted.
Edap TechnomedAug 14, 2017 - Use cautionMedical device
Argo Medical Technologies Ltd recalls ReWalk Personal 6.0. Catalog number: 50-20-0004.
Argo Medical recalls ReWalk Personal 6.0 (catalog 50-20-0004) sold 2015-2017 after injury reports to tibia and fibula. Consumers should check if their device falls within the date range.
Argo MedicalAug 14, 2017 - Lower riskMedical device
Merge Healthcare, Inc. recalls Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare,
Merge Healthcare recalls specific versions of their Unity PACS software due to incorrect Gail Risk calculations for atypical hyperplasia. Affected users must verify their software version and Mammo Tracking license.
Merge HealthcareAug 14, 2017 - Lower riskMedical device
Deerfield Imaging recalls IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw
Deerfield Imaging recalls Starburst adaptor thumb screws with serial numbers 10006657-10006726 due to incorrect thread design. This may cause improper installation and potential safety issues.
Deerfield ImagingAug 14, 2017 - Lower riskFood
NEW SEASONS MARKET recalls Rainbow Carrot and Quinoa Salad, ready to eat product, packaged in one pint clear plastic deli containers, sold at
NEW SEASONS MARKET recalls Rainbow Carrot and Quinoa Salad due to undeclared wheat and pecans in clear plastic containers. Products sold from Aug 13-18, 2017, with UPC 252383-001604.
NEW SEASONS MARKETAug 14, 2017 - Lower riskFood
Dierbergs Markets, Inc Corporate Office recalls Cabernet Grille Butter, Net Wt. 3 OZ, packaged in clear plastic tubs. Dierbergs Kitchens
Dierbergs Markets recalls Cabernet Grille Butter (3 oz clear plastic tubs) due to undeclared wheat and soy. Consumers should check sell-by dates and contact for details.
DierbergsAug 14, 2017 - Stop using nowFood
Garden Of Light Inc. recalls (a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN
Seven Sundays Vanilla Cherry Pecan Muesli is recalled because it contains almonds instead of labeled pecans. Check your UPC and lot codes.
Seven SundaysAug 14, 2017 - Lower riskFood
Kelejete LLC recalls Cranberry Raisin Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane
Kelejete recalls cranberry raisin energy bars due to missing peanut and pecan allergen labels on packaging. The product may contain nut fragments and sulfites from non-GMO apples.
KelejeteAug 13, 2017 - Use cautionMeat & poultry
Luvo Inc. (USA) Recalls Poultry Products Due To Misbranding and Undeclared Allergens
Luvo Inc. recalls 4,805 pounds of poultry products mislabeled as Chicken Chile Verde that contain undeclared allergens like eggs, fish, and soy. Consumers are urged not to consume these products and should discard or return them.
LuvoAug 12, 2017 - Use cautionVehicle
STAR EV SPORT 4+2 (2017) recall — Steering
JH Global recalls 2017 Star EV Sport 4+2 vehicles due to potential tie rod connection failure causing loss of steering control. Owners must have front axle spindle replaced free of charge.
JH GlobalAug 12, 2017 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 2500 (2017) recall — Equipment
Mercedes-Benz Sprinter 2017 models with faulty Kidde fire extinguishers may not function properly during fires, increasing injury risk. Owners must replace extinguishers with a different brand.
Mercedes-Benz SprinterAug 12, 2017 - Use cautionVehicle
KIA SORENTO (2018) recall — Air Bags
Kia is recalling 2018 Sorento vehicles with side curtain air bags that may detach during deployment, posing injury risks. Owners should contact Kia for free replacement.
KiaAug 12, 2017 - Use cautionVehicle
GRAND DESIGN REFLECTION (2018) recall — Equipment
Grand Design is recalling 2017-2018 Reflection and Imagine travel trailers with Smart-Jack power tongue jacks that may crack, causing unintended retraction and potential crashes.
Grand DesignAug 12, 2017 - Use cautionVehicle
FOREST RIVER WILDWOOD (2018) recall — Equipment
Forest River recalls 2018 Wildwood trailers with incorrect tire labels that could cause crashes if wrong tires are installed. Owners must get corrected placards to comply with safety standards.
Forest RiverAug 12, 2017 - Use cautionMedical device
Invivo Corporation recalls Xper Flex Cardio PhysioMonitoring system The Xper Flex Cardio physiomonitoring system is used to facilitate invasive
Invivo recalls Xper Flex Cardio devices with intermittent communication between host system and Flex Cardio. This may cause inaccurate readings during heart and vascular monitoring. Affected models include 453564621791 and :453564621801 (Revision C).
InvivoAug 11, 2017 - Lower riskMedical device
Randox Laboratories recalls Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)
Randox recalls Immunoassay Premium Controls (3x4x5mL and 12x5mL packages) due to ACTH stability claims not meeting specifications. Affected lots include IA2633 (398703, 402366), IA2638 (1666EC), IA2639 (1486EC, 1516EC, 1626EC), and IA2640 (1517EC, 1668EC).
RandoxAug 11, 2017 - UnratedDrug
PD-Rx Pharmaceuticals, Inc. recalls Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count
PD-Rx Pharmaceuticals recalls 15mg Phentermine Capsules due to impurities detected in stability testing. Affected bottles have specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
PD-Rx PharmaceuticalsAug 11, 2017 - Lower riskFood
United Trading Inc. recalls Gazab Green Raisins, 7 oz. 14 oz. packages, 20/25 packs/carton
United Trading Inc. recalls Gazab Green Raisins due to undeclared sulfites in 7oz and 14oz packages sold from November 2016. Consumers should check lot numbers for affected items.
United Trading Inc.Aug 11, 2017 - Lower riskFood
Madhava Honey Ltd recalls Madhava Naturally Sweet Deliciously Organic MMM... Chocolate Chip Cookie Mix,, 13.8 oz. , UPC 0 78314 25105 0. Packaged
Madhava Honey Ltd recalls 13.8 oz. naturally sweet organic chocolate chip cookie mix due to possible undeclared milk. Consumers should check for the UPC 078314251050 and avoid use if allergic.
MadhavaAug 11, 2017 - Lower riskFood
KIND, LLC recalls 4-count boxes of KIND Breakfast Dark Chocolate Cocoa Bars 1.76 oz (50g) Outer Box: UPC: 60265220102-8
KIND recalls 4-count boxes of Breakfast Dark Chocolate Cocoa Bars (UPC 60265220102-8) that may contain protein bars due to mislabeling. Consumers should check their product and contact KIND for details.
KINDAug 11, 2017 - Lower riskFood
Litehouse Inc recalls OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0
Litehouse recalls OPA Greek Yogurt Dressing (item #48246) due to undeclared egg. Consumers should check labels for the UPC 077661150221 and avoid products with egg.
LitehouseAug 11, 2017 - Lower riskFood
Rushing Waters Fisheries, LLC recalls Whole Foods Smoked Whitefish Fillet, packed in bulk boxes. Labeling states: Smoked on: 08/09/17, Sell Through:
Rushing Waters Fisheries recalls Whole Foods Smoked Whitefish Fillets from August 9, 2017, due to potential underprocessing. Consumers should check labels for lot #1139 and stop using if concerned.
Rushing Waters FisheriesAug 11, 2017 - Lower riskMedical device
Med Tec Inc recalls CIVCO Arm Support, REF 106015, distributed as: (a) Rigid Arm Support, Standard, Set Red (PN: 106015) (b) Rigid Adj. Arm
Med Tec recalls CIVCO Arm Supports (PN: 106015) used in Posiboard-2 and Posirest systems due to potential 17mm height difference causing alignment issues during medical treatments.
Med TecAug 10, 2017 - Lower riskMedical device
Aesculap Implant Systems LLC recalls NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of the Vega Knee System Set #ST0468) The affected
Aesculap recalls Vega Knee System component NS357R size T4 due to possible incorrect labeling. Using the wrong size may cause ligament injury, pain, or revision surgery.
AesculapAug 10, 2017 - Lower riskMedical device
Nucletron BV recalls Oncentra Brachy 4.5 radiation therapy software The firm name on the label is Nucletron B.V. Oncentra is a radiation
Nucletron recalls Oncentra Brachy 4.5 radiation therapy software versions 4.5, 4.5.1, and 4.5.2 due to potential incorrect source step size in treatment plans.
NucletronAug 10, 2017 - Lower riskMedical device
Synthes USA recalls Norian Drillable Inject
Synthes recalls Norian Drillable Inject kits with potential expiration date mismatches. Some components expire before the kit's listed expiration date, which could lead to improper use. Affected kits have product number 07.704.010S and lot number DSE0733.
SynthesAug 10, 2017 - Use cautionMedical device
Medline Industries Inc recalls Transfer/Gait Belt, Plastic, Wipeable, packaged in plastic bag, 36 plastic bags per box.
Medline recalls plastic wipeable gait belts with possible slipping when locked. Model MDT821203WPL, lots starting 90317XXXXXX. Stop using if belt slips.
MedlineAug 10, 2017 - Lower riskDrug
Morton Grove Pharmaceuticals, Inc. recalls Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted)
Morton Grove Pharmaceuticals recalls Amoxicillin oral suspension due to customer reports of blue foreign material (nitrile glove) in product. Stop using immediately if you have this specific batch.
Morton Grove PharmaceuticalsAug 10, 2017
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,389 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.