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
35,025 found- Use cautionMeat & poultry
Nestlé Prepared Foods Recalls Not-Ready-to-Eat Pepperoni Hot Pockets Product Due to Possible Foreign Matter Contamination
Nestlé is recalling 762,615 pounds of pepperoni hot pockets with possible glass or hard plastic contamination. Consumers are urged not to eat the product and should dispose of or return it.
NestléJan 15, 2021 - Use cautionVehicle
KZRV SONIC (2021) recall — Equipment
KZRV is recalling 2021 Sonic trailers with a 20-amp circuit breaker instead of 15-amp, which may cause fire. Owners must replace the breaker free of charge by February 22, 2021.
KZRVJan 15, 2021 - Use cautionVehicle
LINCOLN AVIATOR (2020) recall — Visibility
Ford is recalling 2021 Lincoln Aviator vehicles with contaminated windshield washer fluid that may reduce visibility, increasing crash risk. Owners must have system flushed by dealers.
FordJan 15, 2021 - Use cautionVehicle
FORD EDGE (2020) recall — Power Train
Ford is recalling certain 2020-2021 Edge vehicles due to inadequate rear drive unit lubricant, which may cause seizure and loss of vehicle control.
FordJan 15, 2021 - Lower riskMedical device
Medline Industries Inc recalls S-O303000 CONTROL, STAT-SITE B-HB, 2X3ML,1LOW,1HIGH - Product Usage: intended for the quantitative determination of the
Medline recalls specific lots of STAT-Site B-HB controls due to shipment compromise. Affected units may have contamination; contact for replacement.
MedlineJan 15, 2021 - Lower riskMedical device
Biomet, Inc. recalls Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis
Biomet recalls 25mm shoulder screws labeled as 25mm but packaged as 40mm. This mismatch could cause improper implant fixation. Affected units include model 115395 with lot 077170.
BiometJan 15, 2021 - Lower riskMedical device
Qiagen Sciences LLC recalls SARS-CoV-2 Antigen Test
Qiagen recalls SARS-CoV-2 Antigen Test kits with potential for false positives in some patient samples. Learn about affected lots and how to handle the product.
QiagenJan 15, 2021 - Stop using nowMedical device
Hamilton Co recalls HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no
Hamilton recalls heater shakers that may start fires if flammable liquids enter the device. Affected models include HHS2, HHS3, and various adapters. Stop using immediately to prevent fire hazards.
HamiltonJan 15, 2021 - UnratedMedical device
Northgate Technologies, Inc. recalls Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2
Steris recalls CO2MPACT Endoscopic Insufflator systems with specific lot codes due to incorrect tubing material not tested for use. Affected units may pose risks during medical procedures.
SterisJan 15, 2021 - Lower riskMedical device
Medtronic Vascular recalls Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30
Medtronic recalls 6F Launcher Guide Catheter 100 cm EBU 3.0 (LA6EBU30) due to potential sterility compromise from unsealed pouch. Affected units sold with lot code 220857555.
Medtronic VascularJan 15, 2021 - Use cautionMedical device
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 48mm Material Number: 66-348 - Product Usage: intended for
Pioneer Surgical Technology recalls CervAlign Anterior Cervical Plate System (3 Level, 48mm) due to locking mechanism disassociating during surgery or after. Affected units have specific batch numbers.
Pioneer Surgical TechnologyJan 15, 2021 - UnratedDrug
Calvin Scott & Company, Inc. recalls Benzonatate capsules, 100mg, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123,
Calvin Scott recalls 100mg Benzonatate capsules repackaged in 30-count bottles due to label mix-up with Benzphetamine tablets. Affected products contain incorrect medications.
Calvin ScottJan 15, 2021 - Lower riskFood
Piping Rock Health Products recalls FITNESS LABS***Organic***Coconut Oil***Extra Virgin***16 fl. oz. (473 mL)***Carefully Designed and Distributed by
Piping Rock Health Products recalls 16 fl oz organic coconut oil due to potential mold contamination. Consumers should check lot numbers and expiration dates for affected products.
Piping Rock Health ProductsJan 15, 2021 - Lower riskFood
EMILIA FOODS SRL recalls Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Keep Frozen. Needs to be Fully Cooked. UPC 0 85239-10366 1
Emilia Foods recalls Four Cheese Gnocchi (UPC 085239103661) due to possible foreign material. Keep frozen until fully cooked to avoid potential hazards.
Emilia FoodsJan 15, 2021 - Lower riskFood
One Degree Organic Foods Inc, recalls One Degree Organic Foods Gluten Free Sprouted Rolled Oats NET WT. 5 lbs (80 oz) 2.27 kg UPC:6 75625 32318 8
One Degree Organic Foods recalls gluten-free sprouted rolled oats due to rancidity and packaging integrity defects. Check your UPC and Best By date.
One Degree Organic FoodsJan 15, 2021 - Stop using nowFood
Champlain Chocolate Company recalls Gift Baskets 1. Lake Champlain Chocolates - BASKET OF CHEER 2.4lbs - online stock code 1X315-000002-1 UPC:76993305235
Lake Champlain Chocolates recalls gift baskets that may contain plastic pieces. Consumers should check UPC codes and lot numbers for affected items.
Lake Champlain ChocolatesJan 15, 2021 - Use cautionVehicle
HEARTLAND MALLARD (2021) recall — Suspension
Heartland is recalling 2021 Mallard M180BH trailers with incorrect axles, rims, and tires that could cause trailer overload and crash risk. Owners must contact Heartland for free replacement.
HeartlandJan 14, 2021 - Use cautionVehicle
HONDA ODYSSEY (2020) recall — Fuel System, Gasoline
Braun is recalling 2020 Honda Odyssey vehicles with potential fuel leaks that could cause fire. Owners must have their vehicles inspected by dealers for free repairs.
BraunJan 14, 2021 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the
Bard recalls disposable core biopsy instruments with a penetration depth switch that can detach during use, posing a risk of injury. Affected models include MQ1210 to MQK2016 with specific UDI codes and lot numbers.
BardJan 14, 2021 - Lower riskMedical device
Physio-Control, Inc. recalls PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor
Physio-Control
Physio-ControlJan 14, 2021 - Lower riskMedical device
Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and
Ortho-Clinical recalls VITROS VersaTips from specific lots due to deformities that may cause up to 16% sample measurement errors in lab tests. Affected lots include VITROS 250, 350, ECi, 5,1 FS, 3600, 4600, 5600, and XT7600 models.
Ortho-ClinicalJan 14, 2021 - Use cautionFood
Publix Super Markets, Inc. recalls Publix Steam in Bag Season Butternut Medley
Publix recalls Steam in Bag Season Butternut Medley products potentially contaminated with Listeria monocytogenes. Consumers should avoid these items sold between January 3-14, 2021.
PublixJan 14, 2021 - Lower riskFood
Samyang Foods Co Ltd recalls Samyang Buldak Extremely Spicy Hot Chicken Flavor Sauce Hot Chili Sauce Net Wt. 200 g (7.05 oz) Product of Korea UPC: 8
Samyang Foods recalls 200g Hot Chicken Flavor Sauce due to missing egg, milk, and wheat allergen declarations on label. Consumers should check for these ingredients and avoid if allergic.
SamyangJan 14, 2021 - Lower riskFood
Pero Family Farms Company recalls Butternut Veggie Spirals Tray, 10oz, Keep Refrigerated
Pero Family Farms recalls Butternut Veggie Spirals Tray (10oz) due to potential Listeria monocytogenes contamination. Products with specific run numbers from January 15-22, 2021 are affected. Consumers should check labels for affected batches.
Pero Family FarmsJan 14, 2021 - Use cautionConsumer product
Scalpa Recalls Scalpa Numb Maximum Strength Topical Anesthetic Cream Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Scalpa recalls Maximum Strength Topical Anesthetic Cream due to non-child-resistant packaging, risking poisoning for young children. Consumers should stop using, store safely, and get a refund.
ScalpaJan 14, 2021 - Use cautionVehicle
RAM 5500 (2020) recall — Service Brakes, Hydraulic
Braun Northwest recalls 2019-2020 RAM 5500 models with liquid spring suspension for potential rear brake failure. Worn brake lines may leak fluid, causing partial or complete loss of rear brakes. Owners must contact customer service for free repair.
Braun NorthwestJan 13, 2021 - Use cautionVehicle
FREIGHTLINER CASCADIA (2020) recall — Tires
Daimler Trucks North America recalls 2020 Freightliner Cascadia sleeper trucks with specific Bridgestone steer tires due to tread separation or blow-outs causing loss of vehicle control.
Daimler Trucks North AmericaJan 13, 2021 - Use cautionMedical device
Silk Road Medical Inc recalls ENROUTE Transcarotid Stent System REF SR-XXYY-CS
Silk Road Medical recalls ENROUTE Transcarotid Stent System REF SR-XXYY-CS due to tip detachment complaints. Affected units have specific catalog and lot numbers. Contact for remedy.
Silk Road MedicalJan 13, 2021 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated
MedComp recalls Power Injectable CT Port insertion kits with incorrect 6.6F port instead of 5F. This may cause prolonged surgery and increased surgical risks. Affected kits have catalog number MRDP50AXS.
MedCompJan 13, 2021 - UnratedMedical device
BEMER INT. AG recalls Bemer-Set/ Pro-Set for the following models: REF. 410201 (BEMER Pro-Set), REF. 420201 (B.BOX Professional), REF. 420100
BEMER recalls specific models of electromagnetic therapy devices due to potential interference with insulin pumps and pacemakers. Affected models include BEMER Pro-Set and B.BOX Professional series. No remedy is stated in the recall notice.
BEMERJan 13, 2021
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