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
34,943 found- Lower riskMedical device
Luminex Corporation recalls VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro
Luminex recalls VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (five-pack carriers) due to potential false negative results in bacterial detection tests. Affected units include specific supplier and utility tray lots.
LuminexSep 14, 2018 - Lower riskMedical device
LivaNova USA Inc. recalls SORIN Heater-Cooler System 3T, REF 16-02-85 Intended for use with a Stockert/Sorin S3/S5/C5 heart-lung machine and/or
LivaNova recalls six units of SORIN Heater-Cooler System 3T (REF 16-02-85) due to post-deep cleaning water testing positive for nontuberculous mycobacteria. Affected units have specific serial numbers.
LivaNovaSep 14, 2018 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare Millennium MC
GE Healthcare recalls Millennium MC devices with specific system IDs due to risk of detector detachment and falling.
GE HealthcareSep 14, 2018 - Stop using nowMeat & poultry
Bob Evans Farms Inc. Recalls Pork Sausage Link Products due to Possible Foreign Matter Contamination
USDA FSIS recalls 42,246 pounds of Bob Evans Farms pork sausage links (Oct 2018) due to possible clear hard plastic contamination. Consumers urged not to eat these products.
Bob Evans FarmsSep 13, 2018 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Parking Brake
Subaru is recalling certain 2010-2014 Legacy vehicles with manual transmission due to electronic parking brake malfunction that could cause rollaway and crash risk. Owners must contact Subaru for free EPB actuator replacement.
SubaruSep 13, 2018 - Use cautionVehicle
LAND ROVER DISCOVERY (2018) recall — Forward Collision Avoidance
Land Rover is recalling 2018 Discovery vehicles with a potential forward collision avoidance system that may not warn drivers of crashes without intervention.
Land RoverSep 13, 2018 - Use cautionVehicle
KME PREDATOR AERIAL (2018) recall — Exterior Lighting
KME recalls 2018 Predator Aerials with Whelen brake lights that may illuminate without pressing the brake pedal, risking crashes. Owners must have brake lights replaced free by November 2, 2018.
KMESep 13, 2018 - Use cautionVehicle
HONDA CRF250L (2018) recall — Electrical System
Honda recalls 2018 CRF250L motorcycles with electrical system issues that may cause reduced visibility, non-functioning horn, and instrument panel failure, increasing crash risk. Owners must have wiring harness inspected and replaced free of charge.
HondaSep 13, 2018 - Use cautionVehicle
HONDA INSIGHT (2019) recall — Back Over Prevention
Honda recalls 2019 Insight vehicles with faulty rearview camera displays that could increase crash risk. Owners must contact Honda for free software update by October 30, 2018.
HondaSep 13, 2018 - Use cautionVehicle
FOREST RIVER BERKSHIRE (2019) recall — Equipment
Forest River is recalling 2019 Berkshire motorhomes with doors that may open while moving, increasing injury or crash risk. Owners should contact customer service for free door latch adjustments.
Forest RiverSep 13, 2018 - Use cautionVehicle
COACHMEN CATALINA (2019) recall — Suspension
Forest River recalls 2019 Coachmen Catalina and other models due to missing hub bearing races causing overheating and potential axle separation. Owners must contact specified numbers for free hub or axle replacement.
CoachmenSep 13, 2018 - Lower riskMedical device
Abbott Point Of Care Inc. recalls Abbott i-STAT CG8+ Cartridges intended for use in the in vitro quantification of potassium in arterial, venous, or
Abbott recalls i-STAT CG8+ potassium cartridges that may give inaccurate potassium results, especially with low or high potassium samples. Affected units include specific lot numbers and box numbers.
AbbottSep 13, 2018 - Lower riskMedical device
Arthrex, Inc. recalls 3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail
Arthrex recalls 3.2mm Proximal Reamer/Cannulated Drills from FibuLock Nail System packs due to potential breakage during use. Affected units include specific part numbers and serial lots.
ArthrexSep 13, 2018 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188
Terumo recalls its Advanced Perfusion System 1 Electronic Patient Gas System due to outdated service manual for software version 1.30. Affected units may have safety risks.
TerumoSep 13, 2018 - Lower riskMedical device
Roche Diagnostics Corporation recalls CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips, Catalog Number: 04625315160; CoaguChek XS
Roche recalls CoaguChek XS PT test strips with catalog numbers 04625315160, 04625374160, and 07797826160 due to abnormally high INR test results. Affected lots listed in the recall notice.
RocheSep 13, 2018 - Lower riskFood
Lidl US TRADING recalls Bellona brand Milk Chocolate Flavored Coated Wafer with Hazelnut Cr¿me Filling and White Chocolate Flavor, 5.3 oz.
Lidl US voluntarily recalls Bellona brand Milk Chocolate Flavored Coated Wafer with Hazelnut Cr¿me Filling and White Chocolate Flavor due to allergen statement not including wheat. Consumers should check product packaging for UPC 20343613.
Lidl USSep 13, 2018 - Lower riskFood
Ardent Mills, LLC recalls Safeguard Soft Flr (GIV) packaged in 50 lb bags
Ardent Mills recalls Safeguard Soft Flr (GIV) 50lb bags after customer testing found Salmonella. Consumers should check product codes and contact the company for guidance.
Ardent MillsSep 13, 2018 - Lower riskFood
Swanson Health Products, Inc recalls Swanson Ultra, Himalayan Crystal Salt, #SWU403, Net Wt. 35.27 oz. (2.2 lbs) (1,000 grams). Product of Pakistan.
Swanson recalls Himalayan Crystal Salt (35.27 oz) from Pakistan due to potential metal wire pieces. Consumers should check product lot number and contact Swanson for details.
SwansonSep 13, 2018 - Lower riskFood
Brett Anthony Foods recalls Gotham Greens Classic Pesto 6.5 oz. plastic cup, 12 cups per case. Refrigerated. UPC 85392700334
Gotham Greens recalls 6.5 oz. plastic pesto cups (UPC 85392700334) due to ingredient labeling error. The product lists basil, parmesan, and pine nuts but some units show vegan pesto without parmesan.
Gotham GreensSep 13, 2018 - Lower riskMeat & poultry
Roya Foods, LLC Recalls Halal Manti Beef Dumpling Products Produced Without Benefit of Inspection
USDA FSIS recalls approximately 438 pounds of raw Halal Manti Beef Dumplings produced without federal inspection. Consumers are urged not to consume these products and should throw them away or return to retailer.
Roya FoodsSep 12, 2018 - Use cautionMedical device
Howmedica Osteonics Corp. recalls Tritanium TL Steerable Inserter, Cat. No. 48930000, UDI 07613327381900 Product Usage: The TL Steerable Inserter is a
Howmedica recalls Tritanium TL Steerable Inserter (Cat. No. 48930000) due to locking mechanism failure that may cause implant misplacement during spinal surgery.
HowmedicaSep 12, 2018 - Use cautionMedical device
Baxter Healthcare Corporation recalls EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be
Baxter Healthcare recalls EXACTAMIX Empty EVA Bags (250mL) with specific lot numbers due to potential leaking when used for compounding sterile solutions. Affected units may cause solution leakage during medical administration.
Baxter HealthcareSep 12, 2018 - UnratedMedical device
CMP Industries, Llc recalls IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1, Class I, 1 Quart (946ml) REF:3306. Product Usage - Impak Elastic
CMP Industries recalls Impak Elastic Acrylic Resin Liquid Heat Cure Type 1 for foreign material in product. This affects dental splints and nightguards made with specific lot numbers.
CMP IndustriesSep 12, 2018 - Lower riskMedical device
Synthes (USA) Products LLC recalls 3.0mm Headless Compression Screw, Long Thread 18mm, Part Number 04.226.118 DePuy Synthes 3.0mm Headless Compression
Synthes recalls 3.0mm headless compression screws with incorrect thread length (4mm instead of 6mm) that may not fit properly in medical implants.
SynthesSep 12, 2018 - Lower riskDrug
Hetero Labs, Ltd. - Unit III recalls Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway,
Hetero Labs recalls 145mg fenofibrate tablets (Rx only) due to foreign valacyclovir tablets in some bottles. Consumers should check NDC 31722-596-90 and lot E181370.
Hetero LabsSep 12, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Zoledronic Acid Injection, 5 mg/100 mL (0.05 mg/mL) One 100ml Single-Dose Bottle, Rx Only. NOVAPLUS Mfd By: Gland
Dr. Reddy's recalls Zoledronic Acid Injection due to failed impurities testing. This medication may contain harmful substances that could cause health issues. Affected units have specific batch numbers and expiration dates.
Dr. Reddy'sSep 12, 2018 - Lower riskFood
Sarap Asian Fusion recalls Ube Cookies & Cream (cookies); A Sarap Asian Fusion Product; NET WT. 65 G/Cookie; Contains: Flour, eggs, Baking Soda,
Sarap Asian Fusion recalls Ube Cookies & Cream due to undeclared wheat, soy lecithin, and milk. Consumers should check packaging for affected items.
Sarap Asian FusionSep 12, 2018 - Lower riskFood
Swire Coca Cola USA recalls Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
Swire Coca Cola USA recalls Caffeine-Free Barq's Root Beer 12-packs due to mislabeling. Check your cans for the correct lot codes and distribution details.
Barq'sSep 12, 2018 - Stop using nowFood
COCA COLA BOTTLING COMPAN recalls Sprite 12 FL OZ (355 mL) CONTAINS PHENYLALANINE CAFFEINE FREE THE COCA-COLA COMPANY FOR CONSUMER INFORMATION CALL
Coca-Cola Bottling Company recalls specific lots of Sprite 12 oz bottles due to plastic material contamination. Check your UPC and dates.
Coca-ColaSep 12, 2018 - Lower riskFood
Pin Hsiao & Associates, LLC dba Zen Bakery recalls TRADER JOE'S Cinnamon Coffee Cake; NET WT. 16 OZ (1 LB) 454g; SKU# 94235; UPC: 00942355
Zen Bakery recalls Trader Joe's Cinnamon Coffee Cake (SKU 94235) due to undeclared soy lecithin. Consumers should check product labels for the specific lot.
Zen BakerySep 12, 2018
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