Archive
686 recalls were announced in June 2019.
Of the 686 recalls this month scored against our rubric, 2% are Critical, 28% are Severe.
Which agencies issued them
Thor Motor Coach is recalling 1,554 motorhomes because a software defect may cause slide-out rooms to move unexpectedly, increasing injury risk.
Toyota is recalling 2017-2019 Camry, Corolla, RAV4, Sienna, and Yaris iA vehicles because an incorrect load capacity label may lead to unintentional overloading.
Yamaha is recalling about 1,500 Grizzly ATVs and Wolverine X2 ROVs because the owner's manuals contain information for the wrong models.
Honda is recalling specific 2006-2015 models because the passenger frontal air bag inflator may explode due to propellant degradation, posing a risk of serious injury or death.
Honda is recalling specific 2005-2015 Acura and Honda vehicles because driver frontal air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.
Chrysler is recalling 2019 Ram 2500, 3500, 4500, and 5500 diesel trucks because fuel lines may leak, increasing the risk of a fire.
Apple is recalling about 432,000 15-inch MacBook Pro laptops because their batteries can overheat, posing a fire hazard.
Mazda is recalling 2016 MX-5 vehicles because the skid plate and metal bracket may detach, creating a road hazard and increasing crash risk.
Honda is recalling specific Acura and Honda models because the passenger frontal airbag inflator may explode, potentially causing serious injury or death.
Honda is recalling specific Acura and Honda models because driver frontal air bag inflators may explode, posing a risk of serious injury or death.
Fisher-Price is recalling inclined sleeper accessories for Ultra-Lite Day & Night Play Yards due to safety concerns about infant sleep on inclined surfaces.
Dolan Northwest is recalling Design Classics chandeliers because the top loop can break, causing the fixture to fall and pose impact and laceration risks.
Gillette is recalling Venus Simply3 disposable razors because manufacturing errors caused blade misalignment, posing a risk of cuts during normal use.
BRP is recalling Sea-Doo marine coolers because the latch can lock automatically, posing entrapment and suffocation risks. No injuries have been reported.
Mazda is recalling 262,220 vehicles due to a software error that may cause the engine to stall unexpectedly, increasing crash risk.
Maine Wild Blueberry Company is recalling 30-lb cases of frozen wild blueberries after internal sampling detected Listeria monocytogenes. The product was not distributed to consumers.
Bobbie Baby is recalling specific lots of Milk-Based Powder Companion Formula because the product does not provide adequate nutrition for some infants.
Cook Inc. is recalling 131 Advance Enforcer 35 Focal Force PTA Balloon Catheters because multiple complaints reported the balloons bursting below their rated pressure.
Teleflex Medical is voluntarily recalling specific lots of Sheridan LTS tracheal tubes because the 15 mm connector may disconnect from the tube.
Mothers' Milk Bank at Austin is recalling 54 bottles of pasteurized donor human breast milk due to a positive microbiological culture for Bacillus cereus.
FDA is recalling 3,113,280 units of the EGIA 60 Articulating Medical Stapler due to missing pin components that may cause incomplete staple formation and serious surgical complications.
GE Healthcare is recalling 1,113 Discovery IQ PET/CT systems because the table may stop moving while X-ray exposure continues.
Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 0.125 mg due to cross-contamination caused by cleaning failures.
Monarch Medical Technologies is recalling EndoTool IV software versions 1.8 through 1.10 because insulin dosing calculations were erroneously high.
GE Healthcare is recalling 1,113 Optima PET/CT 560 and 560FX systems because the table may stop moving while X-ray exposure continues.
Grandma's Fireworks is recalling 18 types of consumer fireworks because they are overloaded with pyrotechnics, posing explosion and burn risks.
P & L Developments, LLC is recalling 17,664 bottles of Cetirizine Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
APS BioGroup is recalling DPS Throat Spray because testing found elevated levels of Stenotrophomonas maltophilia bacteria.
FDA is recalling 3,113,280 units of the EGIA 60 Curved Tip Art Med Thick Sulu surgical stapler because missing pin components may cause incomplete staple formation and serious medical complications.
The FDA is recalling 3,113,280 units of the EGIA 45 Articulating Xtra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious medical complications.
Cook Inc. is recalling 34 Advance Enforcer 35 Focal Force PTA Balloon Catheters because they may burst below the rated pressure, posing risks of vessel injury and balloon fragmentation.
Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 1.5 mg due to cross-contamination caused by cleaning failures.
Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
GE Healthcare is recalling 1,113 Discovery ML DR PET/CT systems because the table may stop moving without stopping X-ray exposure.
Zydus Pharmaceuticals is recalling Anastrozole tablets due to cross-contamination from cleaning failures. The recall covers 1.4 million bottles distributed nationwide.
Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.
The FDA is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
Whole Foods Market is recalling sun-dried tomato pesto because the labels failed to declare milk, walnuts, and pine nuts.
Ethicon, Inc. is recalling specific lots of ETHIBOND EXCEL polyester sutures because raw materials may contain high endotoxin levels.
FDA is recalling 3.1 million EGIA 45 staplers due to missing pins that may cause incomplete stapling and serious surgical complications.
P & L Developments is recalling 124,512 bottles of Up & Up Children's Cetirizine Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Covidien LLC is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.
Cook Inc. is recalling 73 Advance Enforcer 35 Focal Force PTA Balloon Catheters because they may burst below the rated pressure, posing risks of vessel injury and balloon fragmentation.
Toyota is recalling 2018-2019 Prius C vehicles because a failing DC-DC converter may cause a loss of drive, increasing the risk of a crash.
The FDA is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
Renaissance Food Group LLC is recalling 365 by Whole Foods Yellowfin Tuna Salad due to undeclared soy. The recall covers 144 units sold in Texas, Louisiana, and Oklahoma.
Nissan is recalling 2017-2019 Titan vehicles because a damaged alternator harness may cause an electrical short, increasing the risk of engine stall or fire.
The FDA is recalling 3,113,280 units of EGIA45 CT AR MD THK REL surgical staplers because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
APS BioGroup is recalling Immuno PRP Spray because testing found elevated levels of Stenotrophomonas maltophilia. The product was distributed nationwide and in Switzerland.
P & L Developments, LLC is recalling 202,068 bottles of Cetirizine HCL Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
The FDA is recalling 3,113,280 units of the EGIA 60 Articulating Extra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious surgical complications.
American Health Packaging is recalling 15,386 cartons of Anastrozole Tablets due to potential cross-contamination from cleaning procedure failures.
Subaru is recalling 2019 Legacy and Outback vehicles because improperly applied spot welds may reduce body strength, increasing injury risk in a crash.
The FDA is recalling 3,113,280 units of the EGIA 30 Articulating Medical device due to missing pin components that may cause incomplete staple formation and serious surgical complications.
Preferred Pharmaceuticals is recalling specific lots of Robafen DM cough syrup due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
GE Healthcare is recalling 1,113 Discovery ML PET/CT systems because the table may stop moving without stopping X-ray exposure.
Renaissance Food Group is recalling 365 by Whole Foods Market Classic Tuna Salad Wraps due to undeclared soy. The recall covers 84 units sold in Texas, Louisiana, and Oklahoma.
Teleflex Medical is voluntarily recalling specific lots of Hudson RCI Sheridan tracheal tubes because the 15 mm connector may disconnect from the endotracheal tube.
APS BioGroup is recalling Viralox Immune Balancing Polypeptide Oral Spray because testing found elevated levels of Stenotrophomonas maltophilia bacteria.
Cook Inc. is recalling Zenith Alpha Abdominal Endovascular Grafts that may contain a damaged gray safety lock knob, which could prevent full deployment of the graft.
Stryker GmbH is recalling 447 Endotrac ECTR Hook/Triangle Blade Kits because the sterile bag seal may be compromised, potentially affecting sterility.
Regal Food Inc. is recalling Cornflake flavor Fundraising Cookies because FDA inspection found undeclared wheat, soy, and milk allergens.
GE Healthcare is recalling 119 Vscan Extend ultrasound devices because the LVivo EF app may overestimate ejection fraction values, potentially affecting clinical assessments.
GE Healthcare is recalling 1,113 Discovery PET/CT 610 systems because the table may stop moving while X-ray exposure continues.
MOWI USA LLC is recalling 35 lb cases of Atlantic Salmon because samples tested positive for Listeria monocytogenes. The product is non-ready to eat and must be cooked before consumption.
Wismettac Asian Foods is recalling 40 units of Monaka Belgium Choco & Kurumi Daiichi F in California because the product does not declare coconut as an ingredient or allergen.
Zydus Pharmaceuticals is recalling specific lots of Methylprednisolone tablets due to cross-contamination caused by cleaning failures.
Regal Food Inc. is recalling 40 cases of Regal's Fundraising Cookies (Chocolate Chip) distributed in Oahu, Hawaii, because the label fails to declare wheat, soy, and milk.
Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Butter Almond Toffee because the packaging failed to disclose the presence of almonds and pecans.
Renaissance Food Group LLC is recalling 256 units of Veggie Crudite Bowls with Jicama and Mini Peppers due to undeclared soy. The product was distributed in Texas, Louisiana, and Oklahoma.
Renaissance Food Group LLC is recalling 365 by Whole Foods Market Traditional Egg Salad because it contains undeclared soy.
Bedessee Imports is recalling National Heartland Naturals Pearl Barley because it was mistakenly labeled gluten-free despite containing gluten.
Renaissance Food Group LLC is recalling 365 by Whole Foods Market Smoked Mozzarella Pasta Salad in Texas, Louisiana, and Oklahoma due to undeclared soy.
Gertrude Hawk Brands is recalling R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters because the packaging failed to disclose the presence of almonds and pecans.
Teleflex Medical is voluntarily recalling specific lots of Hudson RCI Sheridan tracheal tubes because the 15 mm Sheridan connector may become disconnected from the endotracheal tube.
Unilever is voluntarily recalling specific Ben & Jerry's Coconut Seven Layer Bar bulk tubs and Chunky Monkey pints because they contain undeclared tree nuts.
Whole Foods Market is recalling Basil Pesto sold in the Northeast because the labels failed to declare milk, walnuts, and pine nuts.
Teleflex Medical is voluntarily recalling specific lots of Hudson RCI Sheridan tracheal tubes because the 15 mm connector may disconnect from the endotracheal tube.
GE Healthcare is recalling 1,113 Discovery PET/CT 710 systems because the table may stop moving without stopping X-ray exposure.
Renaissance Food Group LLC is recalling 365 by Whole Foods Market Classic Potato Salad due to undeclared soy. The product was sold in Texas, Louisiana, and Oklahoma.
Teleflex Medical is voluntarily recalling specific lots of Hudson RCI Sheridan EZ-ENDO endotracheal tubes because the 15 mm Sheridan connector may disconnect from the tube.
Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzels because the packaging failed to list almonds and pecans.
Teleflex Medical is voluntarily recalling specific lots of Sheridan Novaplus endotracheal tubes because the 15 mm Sheridan connector may disconnect from the tube.
Jerr-Dan is recalling 2018-2019 Heavy Duty Wreckers because the remote control system may cause the engine to shut down unexpectedly, increasing crash risk.
Unilever is voluntarily recalling specific Ben & Jerry's ice cream products because they contain undeclared tree nuts, including brazil nuts, hazelnuts, and almonds.
Med Tec Inc is recalling 28 units of the CIVCO Solstice SRS Immobilization System because the device may move during patient setup or treatment.
Patriot Pyrotechnics is recalling 22 types of fireworks because they are overloaded with pyrotechnics, creating explosion and burn risks. No injuries have been reported.
Keystone is recalling G-Force Artillery Shell Fireworks because they are overloaded with pyrotechnics, posing explosion and burn hazards. Consumers should stop using them and return them for a refund.
GS Fireworks is recalling 26 types of consumer fireworks sold in Wyoming, Michigan, because they are overloaded with pyrotechnics, posing explosion and burn risks.
Regal Food Inc. is recalling Regal's Fundraising Cookies because FDA inspection found undeclared wheat, soy, and milk allergens on the label.
Zydus Pharmaceuticals is recalling Pramipexole Dihydrochloride Tablets 0.125 mg due to cross-contamination caused by a cleaning failure.
Gertrude Hawk Brands is recalling R.H. Macy & Co. Dark Chocolate Sea Salt Caramels because the packaging failed to disclose the presence of almonds and pecans.
Ethicon, Inc. is recalling specific lots of Ethibond Excel polyester sutures because raw materials used in manufacturing may contain high endotoxin levels.
The Fresh Group, Ltd. is recalling Maglio Companies Jalapeno Peppers due to potential Salmonella contamination. The product was distributed in five states.
Renaissance Food Group LLC is recalling 274 units of Veggie Crudite Bowls with Asparagus and Bell Peppers due to undeclared soy. The product was distributed in Texas, Louisiana, and Oklahoma.
APS BioGroup is recalling Immulox polypeptide supplements due to elevated levels of Stenotrophomonas maltophilia. The recall covers 7,132 units distributed nationwide and in Switzerland.
Arrow International Inc is recalling 48 units of Arrowg+ard Blue Advance PICC catheters because the product has an incorrect expiration date.
Arrow International Inc. is recalling Arrow JACC devices with Chloraguard Technology due to an incorrect expiration date on the packaging.
Ecolab is recalling 183 cases of QUIK-CARE Aerosol Foam Hand Sanitizer because it was manufactured using the wrong alcohol raw material.
Sun Pharmaceutical is recalling Allergy Relief D tablets because testing showed impurities above or near specification limits.
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