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
Teleflex Medical Europe Ltd recalls Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c)
Teleflex Medical recalls Simplastic suprapubic puncture instruments with latex that may cause allergic reactions. Affected products include specific model codes and batch numbers. Consumers should check packaging for the allergy warning.
Teleflex MedicalMar 15, 2018 - Lower riskDrug
InvaGen Pharmaceuticals, Inc. recalls buPROPion HCl Extended-Release Tablets, USP (SR), 150 mg ,a) 60 count (NDC 69097-878-03) and b) 100 count (NDC
InvaGen Pharmaceuticals recalls 150mg buPROPion HCl Extended-Release Tablets due to failed dissolution testing during stability checks. These prescription pills (NDC 69097-878-03 and 69097-878-07) may not release medication properly.
InvaGenMar 15, 2018 - Lower riskDrug
Bayer HealthCare Pharmaceuticals, Inc. recalls All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual
Bayer recalls Alka-Seltzer Plus packages with green or orange Bayer logo on front carton due to potential ingredient mismatch. Check for logo color to identify affected items.
BayerMar 15, 2018 - Lower riskFood
All American Seasonings, Inc. recalls LOST CAJUN GUMBO BASE, T4014, PACK SIZE 45 lb bag, Blended by ALL AMERICAN SEASONINGS, 10600 E. 54th Ave., Units B & C,
All American Seasonings recalls 45lb Lost Cajun Gumbo Base (Lot 80681, Feb 2018) due to Salmonella contamination. Consumers should avoid using this product to prevent foodborne illness.
All American SeasoningsMar 15, 2018 - Lower riskFood
Raley's Family of Fine Stores recalls RALEY'S PISTACHIO GELATO; 10.58 oz. plastic tub UPC: 46567-02382 Ingredients: rehydrated skimmed milk, sugar, coconut
Raley's recalls pistachio gelato with unapproved color additive sodium copper chlorophyllins. Consumers should check UPC 46567-02382 for affected products.
Raley'sMar 15, 2018 - Lower riskFood
Pepsico Foods International recalls diet Pepsi Classic Diet Pepsi Taste, 12oz cans, sold as a 12 pk, ambient storage.
PepsiCo is recalling specific cases of Diet Pepsi Classic 12oz cans sold in Arizona due to mislabeling issues.
PepsiCoMar 15, 2018 - Stop using nowConsumer product
Southwire Recalls Wi-Fi Switches Due to Fire Hazard
Southwire recalls WiOn Indoor In-wall Wi-Fi Switches due to fire risk from overheating. Consumers must stop using and return switches for $4 replacement or refund.
SouthwireMar 15, 2018 - Stop using nowConsumer product
Louis Garneau Recalls Bicycle Helmets Due to Risk of Head Injury
Louis Garneau recalls certain bicycle helmets that may not meet safety standards, risking head injury. Consumers should stop using and return for free replacement.
Louis GarneauMar 15, 2018 - Use cautionConsumer product
Handi-Craft Recalls Dr. Brown's Lovey Pacifier & Teether Holders Due to Choking Hazard
Handi-Craft recalls Dr. Brown's Lovey pacifier & teether holders with specific lot codes due to choking hazard from detachable snaps. Consumers should stop using and contact for replacement.
Handi-CraftMar 15, 2018 - Stop using nowConsumer product
eheat Recalls Envi Wall Heaters Due to Overheating and Burn Hazard (Recall Alert)
eheat recalls Envi wall heaters due to overheating and burn hazards. Check if your model was sold between July 2015 and August 2016 for a free repair.
eheatMar 15, 2018 - Stop using nowConsumer product
Beanworthy Recalls Combination Battery Chargers/Hand Warmers Due to Fire and Burn Hazard; Sold Exclusively at Amazon.com (Recall Alert)
Beanworthy's EnergyFlux and Slim battery chargers/hand warmers can overheat, causing fire or burns. Stop using immediately and contact for free replacement.
BeanworthyMar 15, 2018 - Use cautionVehicle
MASERATI QUATTROPORTE (2017) recall — Engine And Engine Cooling
Maserati recalls 2017 Quattroporte vehicles with V6 engines due to potential transmission shifting to neutral/park or engine shutdowns at slow speeds, increasing crash risk.
MaseratiMar 14, 2018 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and
BioFire Diagnostics recalls FilmArray BCID Blood Culture Panels with specific BD BACTEC bottles, risking false Proteus results. Affected units include catalog numbers RFIT-ASY-0126 and RFIT-ASY-0127 with certain bottle lots.
BioFire DiagnosticsMar 14, 2018 - Lower riskMedical device
Polymer Technology Systems, Inc. recalls PTS Panels¿ CHOL+GLU Test Strips (REF 1765)
Polymer Technology Systems recalls PTS CHOL+GLU Test Strips (REF 1765) due to potential glucose analyte under-recovery before August 2:2018 shelf life. Affected lots include A705.
Polymer Technology SystemsMar 14, 2018 - Lower riskMedical device
Wright Medical Technology, Inc. recalls WRIGHT, Wright Medical Technology, VALOR(R) Nail, Right, Medium, OD: 10mm, L: 200mm, REF415101020
Wright Medical recalls VALOR Nail (Right, Medium) with potential missing compression screw. Affected units may need repair or replacement to prevent injury.
Wright MedicalMar 14, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect
Implant Direct Sybron recalls dental implants with incorrect cap labeling. The cap may show wrong part numbers but the main vial label is correct. Consumers should check their product details.
Implant DirectMar 14, 2018 - Stop using nowMedical device
Philips Electronics North America Corp. recalls Philips HeartStart FRx AED.
Philips recalls HeartStart FRx AEDs made between Sept 2002 and Feb 2: resistor issue may prevent shock delivery during cardiac emergencies. Affected units have specific serial number patterns.
PhilipsMar 14, 2018 - Lower riskMedical device
Accelerate Diagnostics Inc recalls Accelerate PhenoTest BC kit, Ref #10101018. The firm name on the label is Accelerate Diagnostics, Tucson, AZ. A
Accelerate Diagnostics recalls PhenoTest BC kits with specific lot numbers due to potential false positives for Staphylococcus aureus. Affected kits may give incorrect results, but no remedy is specified in the recall notice.
Accelerate DiagnosticsMar 14, 2018 - Lower riskMedical device
Invivo Corporation recalls PHILIPS Xper Flex Cardio Physiomonitoring System, Model Numbers: 453564241901, 453564483321, 453564621791, and
US1433000052
US1433000052Mar 14, 2018 - Lower riskMedical device
Philips Electronics North America Corporation recalls Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray
Philips recalls Allura Xper R8.x and UNIZ systems with FlexVision monitors due to potential screen freezing during long procedures, which may disrupt imaging. Affected units include specific model numbers and versions.
PhilipsMar 14, 2018 - Lower riskFood
Vietti Acquisitions, LLC recalls Southgate Hot Dog Chili Sauce 15 oz cans UPC 0 71846 95242
Vietti Acquisitions recalls Southgate Hot Dog Chili Sauce 15 oz cans (UPC 07184695242) due to unlisted egg and wheat ingredients that may cause allergic reactions.
Vietti AcquisitionsMar 14, 2018 - Stop using nowFood
Davis Chocolate a division of Deco Chem, Inc. recalls Davis Chocolate Peanut Morsels /Organic Peanut Chips
Davis Chocolate recalls peanut morsels and organic chips due to Listeria monocytogenes. Check lot numbers GMPBMO-25 and GMPBMO-26 for details.
Davis ChocolateMar 14, 2018 - Lower riskFood
Precise Food Ingredients, Inc. recalls Roast Beef Gravy Seasoning Manufacturer's code: PF07040000 packaged in a multi-walled paper bag with poly liner, 28
Precise Food Ingredients recalls Roast Beef Gravy Seasoning (lot WO25251, WO25043) due to potential Salmonella contamination. Consumers should check packaging for the manufacturer's code PF07040000.
Precise Food IngredientsMar 14, 2018 - Lower riskFood
Pepsico Inc recalls diet pepsi caffeine free Classic Diet Pepsi Taste, 12 FL OZ (355 mL), UPC: 0 12000 17230 4
Pepsi recalls 12 fl oz diet Pepsi with aspartame mislabeled as 'aspartame free' on outer packaging. Consumers should check UPC 012000172304 for affected lots.
PepsiMar 14, 2018 - Lower riskFood
Newly Weds Foods Inc recalls Lbs, flv roast dark type, 30 # Boxes
Newly Weds Foods recalls industrial dry seasonings from 2018 due to salmonella contamination from a supplier's recalled yeast. Consumers should check product codes for affected items.
Newly Weds FoodsMar 14, 2018 - Lower riskFood
GRIFFITH FOODS recalls Product Name Lot Number or ID Premix Roasted Chicken 1258969 660025
Griffith Foods is recalling Premix Roasted Chicken with lot number 660025 due to potential Salmonella contamination from a supplier's recalled product. Consumers should avoid eating the affected items.
Griffith FoodsMar 14, 2018 - Stop using nowConsumer product
Radio Flyer Recalls Electric Wagons Due to Injury Hazard
Radio Flyer recalls children's electric wagons with model numbers 3912/3912A due to risk of unintended motor activation causing injury. Affected wagons may need immediate stop use and refund.
Radio FlyerMar 14, 2018 - Use cautionConsumer product
Cameron Company Recalls Children's Tents Due to Laceration Hazard; Sold Exclusively at Home Depot
Cameron Company recalls Playtime Pals Pop-Up Hideaway Hut children's tents due to risk of laceration from splintering fiberglass rods. Return to Home Depot for refund or credit.
Cameron CompanyMar 14, 2018 - Use cautionVehicle
HONDA ODYSSEY (2016) recall — Seats
Honda recalls 2016 Odyssey vehicles with second row left outboard seats that may unlock during crashes, risking injury. Owners must have seatback checked and repaired free by dealers.
HondaMar 13, 2018 - Use cautionMedical device
Medtronic Sofamor Danek USA Inc recalls Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments, DRILL GUIDES: a) REF 6975205, 5mm b) REF
Medtronic recalls cervical disc surgery instruments with drill guides that may break during use, causing potential complications. Affected models include REF 6975205, 6975206, and 6975207 with specific lot numbers.
MedtronicMar 13, 2018
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