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
34,960 found- Use cautionVehicle
DUCATI PANIGALE V4 S (2018) recall — Fuel System, Gasoline
Ducati recalls 2018-2019 Panigale V4 S motorcycles due to fuel spray risk when opening fuel cap, which can cause fire near ignition sources. Owners must update fuel cap venting system.
DucatiMay 20, 2019 - Use cautionVehicle
NEWMAR DUTCH STAR (2020) recall — Service Brakes, Air
Newmar recalls 2020 Dutch Star motorhomes with potential air brake issues causing longer stopping distances. Owners must contact Newmar or Spartan for free brake relay valve replacement.
NewmarMay 20, 2019 - UnratedMedical device
Opternative Inc recalls The Visibly Online Refractive Vision Test which is part of the Visibly Vision Test Solution, This is a software
Opternative Inc recalls its Visibly Online Refractive Vision Test software due to lack of 510K clearance. This software, part of the Visibly Vision Test Solution, requires regulatory approval before use.
Optern: The VisiblyMay 20, 2019 - Lower riskMedical device
Medtronic Inc. recalls Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C used on the iPhone, iPad and iPod Touch devices.
Medtronic recalls Guardian Connect app and transmitter for iPhone/iPad/iPod Touch with iOS 12, causing shorter battery life (4-5 days vs 7+ days).
MedtronicMay 20, 2019 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series
Getinge 86-Series medical washer-disinfectors with part number S-86662003 may have inlet pump hose that collapses during use, causing poor cleaning. Affected units include specific serial numbers.
GetingeMay 20, 2019 - Stop using nowDrug
Teligent Pharma, Inc. recalls Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC
Teligent Pharma recalls 0.05% Betamethasone Dipropionate Ointment due to failed impurities testing. This prescription ointment may cause serious injury if used improperly. Stop using immediately and contact your doctor.
Teligent PharmaMay 20, 2019 - Stop using nowFood
Mothers' Milk Bank at Austin recalls Pasteurized donor human breast milk, Pool 9029, Batch 1 packaged in 3 ounce (90 cc) plastic bottles
Mothers' Milk Bank at Austin recalls Pool 9029, Batch 1 donor breast milk due to positive microbiological culture for bacillus cereus.
Mothers' Milk Bank at AustinMay 20, 2019 - Use cautionFood
Reily Foods Co., Inc recalls Blue Plate Light Mayonnaise 30oz, PET jars
Reily Foods recalls Blue Plate Light Mayonnaise 30oz PET jars due to yeast causing bloating and leakage. Check lot 1904250401.
Blue PlateMay 20, 2019 - UnratedFood
Del Monte Fresh Produce N.A., Inc. HQ recalls Park Street Deli, Hummus and Veggies, Classic Hummus, Carrots & Celery NET WT 5 OZ (142g)
Del Monte recalls Park Street Deli Hummus products due to undeclared peanut butter. Consumers should check for lot number 09129101 and contact Del Monte for details.
Del MonteMay 20, 2019 - Use cautionFood
Suja Life LLC recalls Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 818617020232 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE,
Suja Life LLC recalls Ginger Lemon Kombucha bottles after reports of glass fragments found in the 15.2 oz. glass bottles. Consumers should check UPC 818617020232 for affected items.
SujaMay 20, 2019 - Use cautionMeat & poultry
Vienna Beef Ltd. Recalls Beef Products due to Possible Foreign Matter Contamination
USDA FSIS recalls 2,030 pounds of Vienna Beef frank links products from Illinois, Indiana, and Wisconsin that may contain metal. Food service institutions are urged not to consume these items.
Vienna BeefMay 18, 2019 - Use cautionMeat & poultry
Caito Foods LLC. Recalls Salads with Chicken Products due to Misbranding and Undeclared Allergens
USDA recalls 1,767 pounds of Caito chicken salads due to soy allergen not declared on labels. Consumers urged to discard products purchased between May 12-15, 2019.
Caito FoodsMay 17, 2019 - Lower riskMedical device
Arrow International Inc recalls Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product
Arrow recalls pediatric two-lumen central venous catheter kits with blue flextip catheters due to a labeling error in the lidstock showing reversed gauge values. This may cause incorrect gauge selection during medical procedures.
ArrowMay 17, 2019 - Use cautionMedical device
Beckman Coulter Inc. recalls Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express
Beckman Coulter recalls AU5800XL connection units with serial numbers installed before May 20, 2019 due to potential biohazard exposure from sample splashing. Learn how to check your unit and what to do.
Beckman CoulterMay 17, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity PACS-IW with Universal Viewer version 5.0, Model Number 2068177-001 Product Usage: Centricity Universal
GE Healthcare recalls Centricity PACS-IW with Universal Viewer version 5.0 due to potential missing images in exams without warning. Affected units may display incomplete medical images during radiology procedures.
GE HealthcareMay 17, 2019 - Use cautionMedical device
Covidien LLC recalls EGIA 45 ARTICULATING XTRA THICK SULU, Item Code EGIA45AXT
Covidien recalls EGIA 45 Articulating Xtra Thick Sulu surgical devices that may cause incomplete staple formation, leading to bleeding, infection, or severe complications. Affected units include specific item codes.
CovidienMay 17, 2019 - Lower riskFood
U.S. Tov, Inc. recalls Global Pride Rattan Shoots in Brine: 24 oz. glass jar UPC: 8855273023148 Erawan Enterprise Co. Ltd Bangkok, Thailand.
U.S. Tov, Inc. recalls Global Pride Rattan Shoots in Brine due to high sulfites not declared on label. Products sold in the U.S. with UPC 8855273023148 may be affected.
Global PrideMay 17, 2019 - UnratedFood
House of Spices India, Inc. recalls Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch UPC Code: 2324617054
House of Spices India, Inc. recalls Laxmi Dried Apricots due to elevated sulfites. Consumers should check UPC 2324617054 for affected items.
LaxmiMay 17, 2019 - Lower riskFood
Oakhouse Bakery recalls purely elizabeth Banana Nut Butter Grain-Free Granola, Net Wt. 8 oz. (227g) Re-sealable Pouch. UPC 55140-00272. Made
Oakhouse Bakery recalls Banana Nut Butter Grain-Free Granola pouches due to potential foreign material. Consumers should check UPC 55140-00272 and lot numbers OH01619/OH07219 for affected products.
Oakhouse BakeryMay 17, 2019 - Use cautionVehicle
HONDA PILOT (2015) recall — Air Bags
Honda recalls 2015 Pilot vehicles with potentially improperly installed passenger air bags that may not deploy in crashes, increasing injury risk. Owners must have air bag inspected or replaced free by dealers.
HondaMay 16, 2019 - Lower riskMedical device
Microbiologics Inc recalls Cepheid Xpert C. difficile/Epi Control Panel
Microbiolog: Cepheid Xpert C. difficile/Epi Control Panel has incorrect expiration date (2021-10-31 vs 2021-03-31). Affected units may expire before intended use.
MicrobiologicsMay 16, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls GE Senographe Pristina - Product Usage: Senographe Pristina generates digital mammographic images that can be used for
GE Healthcare recalls specific models of Senographe Pristina mammography machines due to potential slippage of the biopsy positioner during rotation, which could lead to inaccurate procedures.
GE HealthcareMay 16, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging sources, and
GE Healthcare recalls Centricity Universal Viewer 6.0 software versions that may display incorrect patient images from Enterprise Archive or VNA due to missing updated studies. Affected units include specific software versions and model numbers.
GE HealthcareMay 16, 2019 - Lower riskMedical device
Codman & Shurtleff Inc recalls GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
Codman & Shurtleff recalls Galaxy G3 Mini Microcoil Delivery System (Product No: GLM915030) due to incorrect coil length on the label. This may affect medical use safety.
Codman & Shurtle:ffMay 16, 2019 - Lower riskFood
Wismettac Asian Foods, INC recalls CHOCOLATE ALMOND CHOCOLATE MEIJI, 3.1 oz. Item number 64344 UPC 074410643447 - only on those bars with English
Wismettac Asian Foods recalls 3.1 oz Chocolate Almond bars with missing English nutrition labels, ingredients or allergen warnings. Consumers should check for English labeling on bars with Japanese bar codes.
Wismettac Asian FoodsMay 16, 2019 - Stop using nowConsumer product
Meijer Recalls French Fry Cutters Due to Laceration Hazard
Meijer recalls Grand Gourmet french fry cutters with model 54078 due to blade detachment risk of lacerations. Consumers must stop using and return for full refund.
Grand GourmetMay 16, 2019 - Use cautionMeat & poultry
MIBO Fresh Foods LLC Recalls Salad with Meat Products due to Misbranding and Undeclared Allergens
USDA recalls 1,460 pounds of salad with meat products from MIBO Fresh Foods due to undeclared anchovies (allergen) and misbranding. Consumers urged not to consume and dispose of products.
MIBO Fresh FoodsMay 15, 2019 - Lower riskMeat & poultry
Crab House Trading Corp. Recalls Siluriformes Products Produced without Benefit of Inspection
USDA FSIS recalls 49,000 pounds of un-inspected frozen yellow walking fish. Consumers urged not to consume; products should be thrown away or returned to retailer.
Crab House Trading Corp.May 15, 2019 - Use cautionVehicle
IC BUS CESB (2020) recall — Service Brakes, Air
Navistar recalls 2016-2020 school buses with dragging brakes that may activate ABS warning lights, cause sudden stops, or increase fire risk. Owners must have left rear caliper replaced free by dealers.
NavistarMay 15, 2019 - Lower riskMedical device
Medtronic Neuromodulation recalls InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model
Medtronic recalls InterStim systems with model numbers TH90G01, TH90GFA, TH90G02, TH90G03 due to potential unexpected stimulation during programming. Affected users should contact Medtronic for details.
MedtronicMay 15, 2019
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