Archive
921 recalls were announced in July 2016.
Of the 921 recalls this month scored against our rubric, 9% are Critical, 41% are Severe.
Which agencies issued them
Kellogg Company is voluntarily recalling Special K Mini Brownies Fudge due to the potential for undeclared peanut allergen from a supplier's flour recall.
Martinez Imports is recalling 14 cases of Los Mart Chicharrin Lagrima found in New York because testing revealed the presence of undeclared Yellow #6.
Terumo CVS is voluntarily recalling Sarns Dual Cooler-Heater devices because the distributor no longer sells the Inter chlor sanitizer required for cleaning.
DePuy Synthes is voluntarily recalling TFNA Blade/Screw Guide Sleeves because a manufacturing defect may prevent proper use, potentially causing surgical delays.
WalkMed Infusion is recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.
Bayer Healthcare is recalling 42 MEDRAD MRXperion MR Injection Systems because they display a 4205 error message when used with 3T scanners.
CSL Behring is recalling 898 units of Dimension Vista Homocysteine Flex Reagent Cartridges because opened lots show reduced stability and do not meet the 7-day claim.
Martinez Imports is recalling Botanas Los Mart Velitas Candies because samples contained undeclared artificial colors.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Toshiba is recalling 23 Angio WorkStation systems because a software error caused the displayed Peak Skin Dose to be higher than expected during specific procedures.
Terumo CVS is voluntarily recalling Sarns TCM units because the Interchlor sanitizer referenced in cleaning instructions is no longer sold by the distributor.
Siemens Medical Solutions is recalling 50 units of Syngo.via PACS software due to incorrect volume calculation values. A software update is available to resolve the error.
WalkMed Infusion is voluntarily recalling specific IV administration sets due to the potential presence of particulate matter in or on the devices.
Amerx Health Care Corp. is recalling 6,993 units of Amerigel Hydrogel Wound Dressing Advanced Formula because the product did not meet specifications for Zinc Acetate.
Becton, Dickinson and Company is recalling one lot of BD Trucount Absolute Counting Tubes because they may not be sealed properly, which can degrade product performance.
Hologic is recalling 16,870 ATEC Suction Canisters because the lids may crack. These devices are used to collect fluid during breast biopsies.
Martinez Imports is recalling Los Mart Chicharrin Cuadro because testing revealed the product contains undeclared Yellow #6.
The Anspach Effort, Inc. is recalling 18 Anspach G1 High Speed Electric Handpiece Air Cooled units because the graphics indicating locked and unlocked positions are reversed.
Nobel Biocare is recalling 53 Replace Select Tapered dental implants due to incorrect top labels on the packaging. The recall covers units distributed in the US and internationally.
Terumo CVS is voluntarily recalling Sarns TCM II heater-cooler units because the Interchlor sanitizer referenced in cleaning instructions is no longer available.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur XPT system software versions V1.0.1 through V1.1 due to eight identified issues that may affect test results.
Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling 8 varieties of protein drinks because spoilage may cause them to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause them to appear lumpy and have an unpleasant taste and odor.
Martinez Imports is recalling Los Mart Palmex Tornillo wheat flour snacks because sampling revealed undeclared Yellow #6 dye.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Martinez Imports is recalling Los Mart Chicharrin Rueda because sampling revealed the product contains undeclared Yellow #6.
Beckman Coulter is recalling No Foam DxC reagent because it is incompatible with DxC hydropneumatic parts, potentially affecting UniCel DxC System analyzers.
Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Terumo CVS is voluntarily recalling HX2 Temperature Management Systems because the Interchlor sanitizer required for cleaning is no longer available.
Sun Pharmaceutical Industries is recalling 16,085 bottles of Bupropion Hydrochloride Extended Release Tablets because they failed dissolution specifications.
Load Trail is recalling 2014-2016 Triple Axle Tilt Deck trailers because weld joints may crack, potentially causing equipment to disengage and increasing crash risk.
Chrysler is recalling 2015 RAM 2500 and 3500 trucks because inadequate welds on front track bar brackets may separate, reducing steering response and increasing crash risk.
Forest River is recalling 39 Glaval Titan II Low Floor buses due to frames that may crack, potentially reducing driver control and increasing crash risk.
Braun is recalling 2016 MXV vehicles because the passenger seat electrical harness may be crushed, potentially preventing airbag deployment in a crash.
Mahindra is recalling 283 scooters because front forks may not be properly tightened, which can affect low-speed maneuverability and increase crash risk.
Electrolux is recalling about 1,000 Frigidaire and Kenmore electric wall ovens because a malfunctioning thermal switch poses a fire hazard. No injuries have been reported.
Inovonics is recalling about 5,500 emergency transmitters and receivers because they may fail to send or receive help signals. No injuries have been reported.
Aero Industries is recalling Conestoga XP sliding trailer tarping systems because the rear aerodynamic device may separate due to rivet failure, posing a road hazard.
Smocked Threads by Cecil & Lou is recalling about 65 children's nightgowns because they fail to meet federal flammability standards, posing a risk of burn injuries.
Navistar is recalling 2014-2017 International ProStar trucks because a fuse terminal may break, causing total power loss and unexpected engine stalls.
Good Food Concepts, LLC is recalling approximately 2,606 pounds of non-intact beef products from Colorado due to possible E. coli O157:H7 contamination.
PT Farm, LLC is recalling approximately 8,800 pounds of raw beef products due to possible E. coli O157:H7 contamination linked to an illness cluster.
ZF North America is recalling certain 9-speed automatic transmission sensor clusters due to insufficient wire harness crimps that may cause the vehicle to unexpectedly shift to neutral.
BMW is recalling 2016-2017 MINI Clubman vehicles because side curtain air bags may not deploy correctly in a crash, increasing injury risk.
Forest River is recalling specific 2013-2017 recreational vehicles because shower curtains may not resist fire, posing an injury risk.
Forest River is recalling 2017 Coachmen Freedom Express recreational vehicles because insufficient space between the driveshaft and tires may cause tire failure and loss of control.
Mitsubishi is recalling 2015 Outlander Sport vehicles because a CVT hose clamp may not be secured, risking fluid leaks, inoperability, or fire.
Forest River is recalling 2016-2017 Surveyor recreational trailers because the Federal Placard incorrectly classifies them as school buses, posing a crash risk due to potential overloading.
Forest River is recalling 2017 Rockwood and Flagstaff trailers because the tire pressure placard lists 50 PSI instead of the required 65 PSI.
Pierce is recalling 2015-2016 Impel, Enforcer, and Velocity vehicles equipped with aerial devices because a plastic plug may separate, causing a hydraulic leak that disables the device.
House of Smoke is recalling approximately 4,692 pounds of Wild Boar Brotwurst because nitrite levels exceeded regulatory limits. No adverse reactions have been reported.
Kapowsin Meats Inc. is recalling approximately 11,658 pounds of whole hogs for barbeque in Washington due to possible Salmonella contamination linked to an illness outbreak.
Pierce Manufacturing is recalling 2015-2016 Pumper and Tanker trucks because they lack required side marker lights, which may reduce visibility and increase crash risk.
Crosman is recalling rope cocking devices for Centerpoint Sniper 370 crossbows because broken hooks can cause the rope to recoil, posing a laceration risk.
Cycling Sports Group is recalling 2010-2012 Cannondale Bad Boy and Bad Girl commuter bicycles because the fork axle can crack, posing a fall hazard.
Lorex is recalling Care 'N' Share video baby monitors because the lithium polymer batteries can overheat and swell, posing a burn risk.
Nu Skin is recalling Epoch mist diffusers because mold can develop on the product, posing a health risk to individuals with compromised immune systems or mold allergies.
The Kroger Co is recalling Salted Sunflower Kernels because the supplier reported potential Listeria monocytogenes contamination.
Twin City Foods Inc is recalling specific brands of frozen organic mixed vegetables due to potential Listeria monocytogenes contamination. The products were distributed in California, Texas, and Washington.
Dr. Praeger's Sensible Foods is voluntarily recalling frozen Black Bean Burgers because they may be contaminated with Listeria monocytogenes.
The Quaker Oats Company is recalling Quaker Quinoa Granola Bars, Chocolate Nut Medley, because sunflower kernels used in the product are contaminated with Listeria monocytogenes.
The Quaker Oats Company is recalling Quaker Quinoa Granola Bars because sunflower kernels used in the product are contaminated with Listeria monocytogenes.
Twin City Foods is recalling Central Markets Organic Green Peas due to potential Listeria monocytogenes contamination. The products were distributed in California, Texas, and Washington.
Dr. Praeger's Sensible Foods is voluntarily recalling specific lots of frozen Black Bean Burgers because they may be contaminated with Listeria monocytogenes.
Dr. Praeger's is voluntarily recalling California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Dr. Praeger's is voluntarily recalling Organic Harvest Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Heartware, Inc. is recalling 18,631 HeartWare Ventricular Assist System batteries due to premature depletion. The recall covers devices distributed nationwide in the US.
Dr. Praeger's is voluntarily recalling Jumbo California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Medaus, Inc. is recalling B-Complex #3 vials distributed in the U.S., Japan, and New Zealand due to a lack of assurance of sterility.
Dr. Praeger's Sensible Foods is voluntarily recalling frozen California Veggie Balls because they may be contaminated with Listeria monocytogenes.
Medaus, Inc. is recalling M.I.C 25/50/50 vials because the product lacks assurance of sterility. The recall affects 2,000 mL in vials distributed in the U.S., Japan, and New Zealand.
Medaus, Inc. is recalling specific lots of Minoxidil 0.5% vials because the company cannot ensure the product is sterile.
Medaus, Inc. is recalling Pyridoxine HCL 100mg/mL vials because the company cannot assure the sterility of the product.
Medaus, Inc. is recalling Lipo-Injection vials containing methyl B12 and other vitamins due to a lack of assurance of sterility.
Dr. Praeger's Sensible Foods is voluntarily recalling California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Hospira Inc. is recalling 373,850 tubes of Diazepam Injection USP 10mg/2mL because the product contains particulate identified as crystallized active ingredient.
Pharmakon Pharmaceuticals is recalling 45 bags of compounded Midazolam HCI due to a lack of assurance of sterility. The products were distributed nationwide and to specific VA/DOD facilities.
Medaus, Inc. is recalling Hydroxy B12 5mg/mL vials because the company cannot ensure the product is sterile.
Medaus, Inc. is recalling Taurine 50 mg/mL vials because the company cannot assure the product is sterile.
Pharmakon Pharmaceuticals is recalling Phenylephrine 40 mcg/mL injection syringes due to a lack of assurance of sterility.
Medaus, Inc. is recalling specific vials of Pyridoxal/Thiamine/Lidocaine due to a lack of assurance of sterility. The affected products were distributed in the U.S., Japan, and New Zealand.
Medaus, Inc. is recalling specific lots of L-Phenylalanine 15mg/mL vials because the FDA cannot assure the product is sterile.
Medaus, Inc. is recalling Hyaluronidase 500U/ML vials because the company cannot assure the sterility of the product. The recall affects lots distributed in the U.S., Japan, and New Zealand.
Pharmakon Pharmaceuticals is recalling 18 units of Cefazolin 3GM in 0.9% Sodium Chloride bags due to a lack of assurance of sterility.
Pharmakon Pharmaceuticals is recalling 40 units of compounded Promethazine injection due to a lack of assurance of sterility. The product was distributed nationwide to VA and DOD facilities.
Pharmakon Pharmaceuticals is recalling 560 vials of Hydromorphone HCl 0.4mg/mL in 30 mL syringes due to a lack of assurance of sterility.
Medaus, Inc. is recalling Estradiolval and testosterone vials because the company cannot ensure the product is sterile.
Medaus, Inc. is recalling Dexpantenol 250mg/mL vials because the company cannot ensure the product is sterile.
Pharmakon Pharmaceuticals is recalling 75 bags of Fentanyl Citrate injection due to a lack of assurance of sterility. The product was distributed nationwide and to specific VA/DOD facilities.
Pharmakon Pharmaceuticals is recalling 142 units of Provocholine pre-diluted syringes nationwide due to a lack of assurance of sterility.
Medaus, Inc. is recalling specific lots of Folic Acid 10mg/mL vials because the company cannot ensure the product is sterile.
Medaus, Inc. is recalling specific lots of Testosterone Cypionate vials because the company cannot guarantee the product is sterile.
Dr. Praeger's is voluntarily recalling Trader Joe's Quinoa Cowboy Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Medaus, Inc. is recalling specific vials of Methyl B12 injection due to a lack of assurance of sterility. The affected product was distributed in the U.S., Japan, and New Zealand.
Pharmakon Pharmaceuticals is recalling 45 units of Morphine Sulfate IV bags due to a lack of assurance of sterility. The affected products were distributed nationwide and to specific VA/DOD facilities.
Medaus, Inc. is recalling Procaine 2% vials because the company cannot ensure the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Chrysler is recalling 2015-2016 Jeep Renegade vehicles with factory trailer hitches because the assembly may be attached with too few fasteners, increasing crash risk.
Medaus, Inc. is recalling Lipo-Injection vials because the company cannot ensure the product is sterile. The recall covers 5 mL and 10 mL vials distributed in the U.S., Japan, and New Zealand.
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