Archive
758 recalls were announced in June 2017.
Of the 758 recalls this month scored against our rubric, 4% are Critical, 19% are Severe.
Which agencies issued them
Keystone RV is recalling 2018 Dutchmen Coleman trailers because incorrect air conditioner wiring connectors may cause a fire.
Giti Tire is recalling specific Primewell Valera Touring II tires because sidewall cracks may cause air loss and sudden tire failure.
Honda is recalling 2017 Acura MDX Sport Hybrid vehicles because fuel hoses may be misrouted, potentially causing a fuel leak and fire risk.
Newmar is recalling 2014-2018 Dutch Star and 2015-2017 Ventana motorhomes because powered night shades can lower while driving, blocking the driver's view.
KZRV is recalling 2018 Sportsmen LE recreational trailers because they were supplied with spare tires of incorrect size and load capacity, which may fail if used while fully loaded.
Jayco is recalling 2017 Hummingbird travel trailers because tire labels list incorrect pressure requirements, which could lead to tire failure and crashes.
Yamaha is recalling 2017 YZFR3 motorcycles because some may have Canadian certification labels instead of US labels, potentially obscuring safety recall information.
Honda is recalling 2013-2016 Accord vehicles because water intrusion in the battery sensor case may cause an electrical short and increase fire risk.
Design Solutions International is recalling Home Decorators Collection Comotti vanity fixtures because glass shades can detach and fall, posing laceration and burn risks.
Mazda is recalling 2007-2011 CX-7, CX-9, and 2009-2011 Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Newmar is recalling 2018 London Aire, King Aire, and Essex motorhomes because a fuel pump drive gear could slip, causing an engine stall and increasing crash risk.
General Motors is recalling 2016-2017 Buick Envision vehicles because replacement headliners may lack required impact-absorbing foam, increasing injury risk in crashes.
Toyota is recalling 2017 Lexus ES350 vehicles because the right-hand tie rod lock nut may loosen, potentially causing loss of steering and increasing crash risk.
Honda is recalling 2007-2011 CR-V vehicles where the passenger air bag inflator may have an incorrect wire harness, potentially preventing deployment in a crash.
Aston Martin is recalling 2017 DB11 vehicles because the tire pressure monitoring system may fail to warn drivers of low tire pressure, increasing crash risk.
General Motors is recalling 2014 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because they may experience a temporary loss of electric power steering assist, increasing crash risk.
Toyota is recalling 2016 Tundra vehicles because incorrect bolts were used to attach the passenger knee air bag module, which may loosen over time and affect air bag performance during a crash.
Burt's Bees Baby is recalling about 8,500 infant coveralls because the crotch snaps can detach, posing a choking hazard to infants.
South Shore Industries is recalling about 68,300 Summer Breeze style 5-drawer chests because they are unstable and can tip over if not anchored to the wall. Consumers should stop using the chests until they are secured or contact the company for a refund or free restraint kit.
Homestar North America is recalling about 1,470 Stockholm three-drawer TV chests sold at Target.com because they pose serious tip-over and entrapment hazards to children if not anchored to the wall.
Lakota Corporation is recalling 2018 Colt trailers because the furnace flue may be improperly installed, preventing proper venting. This defect can cause carbon monoxide buildup inside the trailer, posing a risk of injury or death.
Vinh Hoan USA is recalling approximately 84,000 pounds of frozen Swai fillets that entered U.S. commerce without meeting federal import requirements.
DePuy Mitek is recalling LATARJET Coracoid Top Hat Drills because the Combo Screw Driver tip may break during surgery.
Vi-Jon, Inc. is recalling 52,212 bottles of Magnesium Citrate Saline Laxative because glass particles were found in the product.
Genetic Edge Compounds LLC is recalling GEC TNT Thermanite dietary supplements because the product contains DMAA and Methylsynephrine.
Monfitello is recalling Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste because it may contain peanuts. Consumers should stop using the product.
H & C Food Inc is recalling 300 cases of Lobster Flavored Balls distributed in New York because the product may contain undeclared egg.
DePuy Mitek is recalling LATARJET Coracoid Drills because the Combo Screw Driver tip may break during surgery.
Blue Diamond Growers is recalling blanched diced almonds after a customer reported a positive Salmonella test result upon receipt.
Herbmed USA Company Inc. is recalling NutriHeal OPTIMAL CHOLESTEROL herbal supplements because they contain undeclared milk.
DeMoulas Supermarket, Inc. is recalling Market Basket moreBAR Dark Chocolate Peanut bars because they contain undeclared walnuts.
Ion Beam Applications S.A. is recalling 18 Proteus 235 systems due to potential dark current issues in Pencil Beam Scanning mode.
Omega Medical Imaging is recalling 6 units of 2 over 2 Elevating Monitor Suspension pillars because the column may drop and fail to rise.
DePuy Mitek is recalling 115 units of the LATARJET EXPERIENCE Extraction Driver because the tip may break during surgery when used at an angle.
DePuy Mitek is recalling 153 units of the LATARJET EXPERIENCE Top Hat Tap because the Combo Screw Driver tip may break during surgery.
Lance is recalling 2018 Travel Trailers with optional utility receivers that have insufficient welds, which may cause attached items to contact the road.
Kovatch Mobile Equipment is recalling one 2017 KME Predator Tanker truck because a fuel pump drive gear may slip, causing an engine stall that increases crash risk.
DePuy Mitek is recalling 173 LATARJET Combo Screw Drivers because the tip may break during surgery when used at an angle.
Joseph Shalhoub & Son, Inc. is recalling Joray Fruit Punch fruit rolls because they contain undeclared wheat. The product was distributed in New York and Florida.
Hail Merry LLC is recalling Meyer Lemon Miracle Mini Tarts due to undeclared cashews. Consumers should check for specific lot codes.
Medtronic is recalling 65,959 MiniMed 630G insulin pumps because the device may become temporarily stuck and the keypad may become unresponsive.
Medtronic is recalling 117,239 MiniMed 670G insulin pumps because the keypad may become unresponsive and the pump may become temporarily stuck.
Medtronic is recalling 6,573 MiniMed 620G insulin infusion pumps because the keypad may become unresponsive and the pump may become temporarily stuck.
Star Snacks Co. is recalling Southern Grove Cashew Halves & Pieces with Sea Salt because a consumer found a glass fragment in the product.
Vascular Solutions, Inc. is voluntarily recalling Venture RX, OTW, and CS catheters because material may detach from the distal tip during use.
Monfitello is recalling Private Selection African-Inspired Peri Peri Chili Culinary Spice Paste because the product may contain peanuts.
Medtronic is recalling 117,239 MiniMed 640G insulin pumps because the keypad may become unresponsive, potentially preventing users from adjusting insulin delivery.
Meijer is recalling Honey Vanilla Bourbon Pecans because the label incorrectly lists cream, milk, and eggs, while omitting other ingredients.
Publix Super Markets is recalling 16-ounce Artichoke & Spinach dip due to potential glass fragments. The product was distributed to six southeastern states.
Siemens is recalling Dimension Vista TSH reagent cartridges because the instructions for use list incorrect units and interference levels for biotin.
Siemens Healthcare Diagnostics is recalling Dimension Vista Prolactin reagent cartridges because the instructions for use contain incorrect biotin interference data.
Merge Healthcare is recalling Merge OrthoPACS software versions 6.6, 6.6.1, and 6.6.2 because prior studies may fail to display annotations.
Z-Medica is recalling 2,910 units of QuikClot TraumaPad hemostatic dressings because packaging breaches may compromise sterility.
Abbott Laboratories is recalling 7,981 kits of ARCHITECT SHBG Reagent because using Potassium EDTA specimen tubes may cause falsely decreased test results.
Siemens Healthcare Diagnostics is recalling Dimension Vista Estradiol reagent cartridges because the instructions for use contain incorrect biotin interference units.
Lucid Pharma LLC is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, because pharmacists reported bottles containing melted capsules.
Siemens Healthcare Diagnostics is recalling Dimension Vista Ferritin reagent cartridges because the instructions for use contain incorrect units and levels for biotin interference.
Merge Healthcare is recalling specific versions of Merge OrthoPACS software because studies may fail to transfer or import correctly between servers.
Siemens Healthcare Diagnostics is recalling Dimension Vista Digoxin reagent cartridges because the instructions for use contain incorrect units and levels for biotin interference.
Siemens is recalling Dimension Troponin 1 reagent cartridges because the instructions for use list incorrect units and interference levels for biotin.
American Promotional Events is recalling TNT Red, White, & Blue Smoke fireworks because they can explode unexpectedly, causing burn injuries.
Spartan Motors is recalling 2017-2018 K3, K4, and Gladiator chassis because a fuel pump gear may slip, causing engine stalls that increase crash risk.
General Motors is recalling 2016-2017 Buick Envision vehicles because incorrectly installed tablet holders may prevent head restraints from fully engaging, increasing injury risk in a crash.
Triple E RV is recalling 35 units of the 2017 Wonder motorhome because the water heater door can block the furnace, increasing fire risk.
Transportation Collaborative is recalling 2012-2017 Trans Tech buses because a fuse in the air conditioning system may short, overheat, and cause a fire.
Ford is recalling 2016 Escape vehicles because the driver's knee airbag may not inflate properly in a crash, increasing injury risk.
Daimler Trucks North America is recalling 2015-2017 Freightliner models because a missing check valve could cause sudden parking brake application and increase crash risk.
Ford is recalling 2015-2017 Transit vehicles because a flexible coupling may fail, potentially damaging brake and fuel lines or allowing the vehicle to roll.
Ford is recalling 2017 Explorer Police Interceptor vehicles because second-row seats may lack front inboard attachments, failing federal safety standards and increasing crash injury risk.
Volkswagen Group of America is recalling 2016-2017 Audi Q3 vehicles because brake lights may not activate during emergency braking if the parking brake is engaged.
Overhill Farms is recalling approximately 54,630 pounds of frozen chicken bites products due to possible contamination with bone fragments.
Maxi Canada, Inc. is recalling 4.3 million pounds of frozen breaded chicken products because they may contain undeclared milk, a known allergen.
The Wornick Company is recalling beef ravioli products because they may contain undeclared milk, a known allergen, which is not listed on the label.
Honda is recalling 2018 Odyssey vehicles because the third-row center seat belt tongue may not latch securely, increasing injury risk in a crash.
Forest River is recalling 2014-2018 Coachmen RV models because exposed wiring may short circuit and cause a fire.
Continental Automotive Systems is recalling fuel pump flanges for Volkswagen, Audi, and Porsche vehicles because they may crack and leak fuel, increasing fire risk.
Mazda is recalling 2014-2016 Mazda3 and Mazda6 vehicles because water may cause the parking brake actuator shaft to corrode and bind, potentially preventing the brake from engaging or disengaging fully.
Jaguar is recalling 2010-2011 XJ vehicles because a software update failure may leave air bag calibration incorrect, increasing injury risk in a crash.
Complete Pharmacy and Medical Solutions LLC is recalling 1,890 syringes of Human Chorionic Gonadotropin (HCG) due to confirmed mold contamination.
L.A. Lucky Import & Export is recalling sweet basil seeds from Vietnam after Salmonella was found in a related shipment.
Complete Pharmacy and Medical Solutions LLC is recalling 49 vials of Human Chorionic Gonadotropin due to confirmed bacterial contamination.
The Kroger Co is recalling Simple Truth Dry Roasted Macadamia Nuts due to potential Listeria monocytogenes contamination.
Creganna Medical Devices is recalling 50 units of Boston Scientific Zurpaz Steerable Sheaths due to a lack of sterility assurance.
Safecor Health LLC is recalling 856 bottles of Doxycycline 100mg tablets in Massachusetts and New York due to Current Good Manufacturing Practice (CGMP) deviations.
Aston Martin is recalling 2012 V8 Vantage vehicles because a transmission connector may break, causing a fluid leak that could prevent shifting or cause the vehicle to roll away.
Creganna Medical Devices is recalling 85 units of Boston Scientific Zurpaz Steerable Sheaths due to a lack of sterility assurance.
The Horton Fruit Co is recalling specific bags and totes of spinach sold as Harris Teeter and Peak brands due to possible listeria contamination.
Aston Martin is recalling 2011-2014 V8 Vantage vehicles because a broken clutch fluid line connector may cause hydraulic leaks, preventing gear shifting or causing the vehicle to roll away.
Gilster-Mary Lee Corp. is recalling Western Family Onion Soup Mix because it may contain undeclared egg. The product was distributed to Associated Foods Stores in Utah.
GE Healthcare is recalling Infant Warmer Systems because loose screws in the heater head could fall and cause thermal injuries to patients.
Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.
Bright Farms is recalling 4oz packages of Baby Romaine salad due to detected metal contamination. The firm identified the issue through internal verification.
Medtronic is recalling custom suture packs because an incomplete inner package seal may cause the suture material to degrade prematurely.
Bright Farms is recalling Spring Mix salad products in 4 oz. and 8 oz. packages because metal was detected in the product.
Woodland Foods is recalling D'Allesandro De-stemmed Birdseye Chiles because trace amounts of undeclared peanut were found in the product.
GE Healthcare is recalling 10,884 BrightSpeed X-ray systems because a defect may cause scans to start before a prescribed delay completes.
Bright Farms is recalling Thai Basil packages due to detected metal contamination. The firm identified the issue through internal verification.
Biomerieux Inc is recalling VITEK 2 Gram Positive Susceptibility cards because compromised container integrity may expose the product to moisture, potentially degrading antibiotic potency.
Cook Inc. is recalling 29 Pereyra Ligature Carrier 75 devices because their reprocessing instructions do not provide sufficient detail for cleaning, disinfection, and sterilization.
Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, potentially causing antibiotic degradation.
Looking for a different month? Back to 2017.