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
Halyard Health, Inc recalls Halyard Closed Suction System for Adults, Turbo- cleaning¿Closed¿Suction¿System¿for¿Adults,¿Double¿Swivel¿Elbow (DSE).
Halyard Health recalls adult suction systems with Flex Connectors that may become loose or disconnect before or during use, posing a risk of disconnection. Check product details to see if your unit is affected.
Halyard HealthFeb 7, 2018 - UnratedDrug
Webrx dba RxPalace.com recalls BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by
RxPalace recalls BonaDur For Men lidocaine spray due to manufacturing deviations. Products may not meet current good manufacturing practices standards.
RxPalaceFeb 7, 2018 - Lower riskDrug
Pfizer Inc. recalls Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation.
Pfizer recalls 10 mg/mL hydromorphone injection vials that may be empty or cracked, posing a risk of contamination. Affected vials have specific NDC and expiration dates.
PfizerFeb 7, 2018 - Lower riskMeat & poultry
Olymel S.E.C./ L.P. Recalls Pork Products Produced Without Benefit of Import Inspection
U.S. Department of Agriculture recalls 4,618 pounds of raw pork products imported from Canada without U.S. re-inspection. Consumers urged not to consume these products.
OlymelFeb 6, 2018 - Lower riskMeat & poultry
Guymon Extracts, Inc. Recalls Fully Cooked Pork Products Due to Possible Processing Deviation
Guymon Extracts recalls 4,202 pounds of fully cooked pork products from Jan. 3, 2018, due to potential spore-forming pathogen growth including botulism-causing bacteria. Consumers should check labels for lot code 010218-1.
Guymon ExtractsFeb 6, 2018 - Lower riskMedical device
Baxter Healthcare Corporation recalls Sterile EXACTAMED Oral Dispenser, Clear, Individually Packaged, 5 mL, Product Code H93876105
Baxter recalls sterile 5mL oral dispensers with mislabeled product codes and volumes. Affected units may have incorrect labeling that could lead to improper use.
Baxter HealthcareFeb 6, 2018 - Use cautionMedical device
Zimmer Biomet, Inc. recalls AIM Tibial Nails intramedullary fixation rod - NON-STERILE; Item numbers: 810508255 NAIL TIB DYN 08 X 25.5 810508270
Zimmer Biomet recalls AIM Tibial Nails intramedullary fixation rods due to high surgical revision rates. These non-sterile rods require sterilization before use and are affected by specific item numbers.
Zimmer BiometFeb 6, 2018 - Lower riskFood
La Salsa Foods Inc recalls Pepitas - International Food Court brand, Thai Sweet Chili Roasted Pumpkin Kernels, 4 oz. vacuum sealed plastic bag,
La Salsa Foods Inc recalls Thai Sweet Chili Roasted Pumpkin Kernels due to undeclared soybean oil and soy lecithin in the product. Consumers should check labels for the specific product and contact the company for details.
International Food CourtFeb 6, 2018 - Lower riskFood
WEIS MARKETS recalls Weis Weis Markets, Inc., Sunbury, PA 17801-0471; Keep Refrigerated; Dried Beef Party Rye Dip; Ingredients: Hellman's
Weis Markets recalls Dried Beef Party Rye Dip due to undeclared egg and milk in ingredients. This may cause allergic reactions for those with egg or milk allergies. Check your product's sell-by date and contact Weis Markets for details.
Weis MarketsFeb 6, 2018 - Stop using nowConsumer product
Tiffany & Co. Recalls Crystal Mugs Due to Burn and Laceration Hazards (Recall Alert)
Tiffany & Co. recalls 11 oz Wheat Leaf crystal mugs due to burn and laceration hazards when used with hot liquids. Get a refund and $100 gift card.
Tiffany & Co.Feb 6, 2018 - Use cautionConsumer product
Lenovo Recalls ThinkPad Laptops Due to Fire Hazard
Lenovo recalls 14-inch ThinkPad X1 Carbon 5th Generation laptops (2016-2017) due to fire hazard from unfastened screws damaging batteries. Affected units must be inspected and repaired.
LenovoFeb 6, 2018 - Stop using nowConsumer product
Kohler Recalls Gasoline Engines Due to Risk of Fuel Leak and Fire Hazard (Recall Alert)
Kohler recalls gasoline engines SH265, CH245, CH255, CH270, CH395, CH440, and ECH440 models due to faulty fuel caps that can cause fuel leaks and fire hazards. Consumers should stop using and contact Kohler for free repairs.
KohlerFeb 6, 2018 - Use cautionVehicle
THOR MOTOR COACH TUSCANY (2017) recall — Steering
Thor Motor Coach recalls 2011-2017 Tuscany motorhomes with faulty power steering hoses that may cause electrical arcing and fire if power steering fluid leaks.
Thor Motor CoachFeb 5, 2018 - Use cautionVehicle
WINNEBAGO REVEL (2018) recall — Equipment
Winnebago recalls 2018 Revel RVs with roof racks that may detach while moving, causing road hazards and crash risks. Owners must contact Winnebago for free fix by May 29, 2018.
WinnebagoFeb 5, 2018 - Use cautionVehicle
VOLKSWAGEN ATLAS (2018) recall — Fuel System, Gasoline
Volkswagen is recalling 2018 Atlas vehicles with a fuel tank leak risk that could cause fire. Owners must have the fuel tank replaced free by dealers by June 22, 2018.
VolkswagenFeb 5, 2018 - Lower riskMedical device
Hyphen BioMed recalls ZYMUTEST HIA MonoStria qualitative screening assay intended for the global detection of heparin-dependent antibodies,
Hyphen BioMed recalls ZYMUTEST HIA MonoStria kits for heparin-dependent antibody testing due to incorrect package instructions about plasma use. Affected kits should only be used with plasma, not serum or other fluids.
Hyphen BioMedFeb 5, 2018 - Lower riskMedical device
ICU Medical, Inc. recalls 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear, NanoClave¿ T-Connector, Clamp, Rotating Luer, Bulk
ICU Medical recalls 6.5" smallbore infusion sets with incorrect spin collars. These devices may cause improper connections during medical use. Affected units include specific lot numbers and model A1009-NS.
ICU MedicalFeb 5, 2018 - Lower riskDrug
Teva Pharmaceuticals USA recalls Fluoxetine Tablets USP, 10 mg, 30-count bottle, Rx only, Manufactured in Israel by: Teva Pharmaceuticals IND, LTD,
Teva Pharmaceuticals USA recalls 10mg fluoxetine tablets due to impurities found in stability testing. Affected products may have unsafe levels of lactoside. Contact for return instructions.
Teva PharmaceuticalsFeb 5, 2018 - Lower riskDrug
PharMEDium Services, LLC recalls 0.2% Ropivacaine HCI (Preservative Free) in 0.9 Sodium Chloride, Epidural, 250 mL Yellow Cassette, Rx only, PharMEDium
PharMEDium recalls 250mL epidural anesthetic cassettes due to potential sterility issues. Product may be contaminated with endotoxins from improper testing.
PharMEDiumFeb 5, 2018 - Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray), 30 mL, Rx only, Distributed by: Sun
Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution 0.1% (30mL) due to droplet size test failure during stability testing. This may affect drug consistency but does not pose immediate safety risks.
Sun PharmaceuticalFeb 5, 2018 - Lower riskDrug
Genentech, Inc. recalls Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A
Genentech recalls 0.5mg Klonopin tablets due to missing Schedule IV controlled substance label on packaging. This could lead to improper use or diversion. Check your product details and contact Genentech for instructions.
GenentechFeb 5, 2018 - Lower riskFood
eBars recalls DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064
eBars recalls DIABEATIC Chocolate Berry Crunch bars due to undeclared peanuts. All products are affected. Consumers should check for peanuts if allergic.
eBarsFeb 5, 2018 - Use cautionFood
Meijer Distribution, Inc recalls Meijer Greek Yogurt 0% Blueberry 5.3 oz. The products are packaged in a plastic cup with a foil seal and a label
Meijer recalls Greek yogurt with potential glass particles. Consumers should check UPCs and stop using if glass is found.
MeijerFeb 5, 2018 - Stop using nowConsumer product
B & P Lamp Supply Recalls Lamp Sockets Due to Fire Hazard
Golo recalls brown 3-way lamp sockets (GE-8015) due to fire hazard. Stop using, disconnect, and return for a refund or replacement.
GoloFeb 5, 2018 - Use cautionVehicle
CROSSROADS ZINGER (2018) recall — Equipment
Keystone is recalling 2018 Crossroads Zinger trailers with Norcold N306 refrigerators that may have a loose or missing propane gas valve test port screw, risking fire if used in gas mode.
KeystoneFeb 3, 2018 - Use cautionVehicle
TRIPLE E RV REGENCY GT (2010) recall — Equipment
Triple E is recalling 2010 Regency GT RVs with potentially clogged Kidde fire extinguishers that may fail during fires, increasing injury risk. Owners must contact Kidde for free replacement.
Triple EFeb 2, 2018 - Use cautionVehicle
LANCE TRAVEL TRAILER (2018) recall — Electrical System
Lance is recalling 2018 travel trailers with model numbers 1985, 1995, 2185, 2155, 2295, and 2375 due to risk of battery falling out while towing, potentially causing crashes.
LanceFeb 2, 2018 - Use cautionVehicle
KENWORTH T680 (2018) recall — Electrical System
PACCAR recalls 2017-2018 Kenworth T680 and T880 trucks with faulty transmission displays that may cause the truck to not move, violating safety standards.
KenworthFeb 2, 2018 - Use cautionVehicle
JAGUAR XE (2018) recall — Fuel System, Gasoline
Jaguar recalls 2018 XE vehicles with 2.0L gasoline engines due to potential fuel leaks in engine bays that could cause fire near hot engine parts.
JaguarFeb 2, 2018 - Lower riskMedical device
Philips Consumer Lifestyle recalls Philips Avent Smart Ear Thermometer (SCH740), Philips Ear Thermometer (DL8740)
Philips recalls two ear thermometers due to potential inaccurate temperature readings. Affected models include SCH740 and DL8740. No specific remedy is provided in the recall notice.
Philips Consumer LifestyleFeb 2, 2018
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