Archive
908 recalls were announced in November 2014.
Of the 908 recalls this month scored against our rubric, 2% are Critical, 20% are Severe.
Which agencies issued them
Chrysler is recalling 11,674 2015 Dodge Challengers because the instrument cluster may become inoperative, increasing crash risk.
Ranchers Legacy Meat Co. is recalling 1,200 pounds of ground beef products produced on Nov. 19, 2014, due to possible E. coli O157:H7 contamination.
Mitsubishi is recalling 2013-2015 Outlander Sport vehicles because the front passenger seat belt fastener may loosen, increasing injury risk in a crash.
Terex is recalling 84 model year 2014 Light Tower AL5 work platforms because insufficient structural support on the fuel tank could cause it to deform and contact the trailer axle, increasing fire risk.
Altec is recalling 1999-2014 aerial devices because an improperly set hydraulic pressure transducer may cause inadvertent boom movement in cooler temperatures, increasing injury risk.
Graco is recalling 11 stroller models because the folding hinge can pinch a child's finger, causing lacerations or amputations.
Mack Trucks is recalling 2015 Pinnacle and Granite trucks because an incorrectly wired system may fail to control engine speed, increasing the risk of fire.
Tyco is recalling about 750 Simplex 4100ES fire alarm control panels because a defective chip can prevent the system from activating during an alarm, posing a risk of injury and property damage.
Bob-Cat is recalling about 4,900 zero turn riding mowers because the steering control arm can break, causing the driver to lose control and crash.
Leatherman is recalling the Leap multi-tool because the optional knife blade can inadvertently release, posing a laceration hazard. No injuries have been reported.
Maine Natural Health, Inc. is recalling Fortified Vanilla Dietary Supplement because it fails to declare milk as an allergen.
Siemens Healthcare Diagnostics is recalling Rapid Neg Urine Combo Panel Type 1 due to an increase in false positive susceptible results when used with MicroScan Microbiology Systems.
Z Natural Foods is recalling Lightly Roasted Organic Carob Powder due to a possible risk of Salmonella contamination.
GE Healthcare is recalling Infinia nuclear medicine systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.
Exotic Superfoods New York, Inc. is recalling specific lots of 100% Raw Young Thai Coconut Water because the batches were not subjected to the required 5-log reduction processing.
Maine Natural Health, Inc. is recalling fortified chocolate dietary supplements because they fail to declare the allergen milk. The products are sold nationwide in 2 lb and 10 oz sizes.
Maine Natural Health, Inc. is recalling Hunger and Weight Vanilla dietary supplements because they fail to declare the milk allergen.
Philips is recalling 22 Allura Xper FD20C radiological imaging systems due to a faulty Automatic Motion Controller that may cause hazardous movement of the C-arc.
Philips Medical Systems is recalling two Allura Xper FD20C systems due to a faulty Automatic Motion Controller that may cause hazardous C-arc movement.
Maine Natural Health, Inc. is recalling Endurance Pre Race Lime dietary supplement because it fails to declare milk and shellfish allergens.
AP Specialties is recalling about 172,000 Two-Tone Power Bank Chargers because they can overheat and cause a fire. Consumers should stop using the units and contact the company for a replacement.
Fisher and Paykel Healthcare is recalling IW900-Series Infant Warmers and spare parts because a broken nut may allow the heater head to swing and injure infants.
GE Healthcare is recalling 255 Discovery NM/CT 670 systems because loose fasteners may cause a portion of the system to fall onto patients during scans.
Maine Natural Health, Inc. is recalling Pure Whey Natural Dietary Supplement because the product fails to declare the allergen milk on the label.
GE Healthcare is recalling 29 Optima NM/CT 640 systems because loose fasteners could cause the camera to fall onto a patient during a scan.
Maine Natural Health, Inc. is recalling Endurance In Race Coconut Dietary Supplement because it fails to declare the allergen milk.
Maine Natural Health, Inc. is recalling Daily Balance Chocolate Dietary Supplement because it fails to declare the milk allergen.
Maine Natural Health is recalling Hunger and Weight Chocolate Dietary Supplement because it fails to declare the milk allergen.
Medacta is recalling GMK Intramedullary Extension Rods 100 mm after three reported cases of breakage during total knee replacement surgeries.
Maine Natural Health, Inc. is recalling Daily Balance Vanilla dietary supplements because they fail to declare the allergen milk. The recall covers 2 lb and 10 oz sizes distributed nationwide.
Maine Natural Health, Inc. is recalling Rejuvenate Vanilla Dietary Supplement because it fails to declare the allergen milk. The product was distributed nationwide in 2 lb and 10 oz sizes.
Maine Natural Health, Inc. is recalling Endurance In Race Lime Dietary Supplement because it fails to declare milk and coconut allergens.
Fabrique Delices recalls 14 pounds of garlic sausage due to misbranding and undeclared nonfat dry milk. No adverse reactions have been reported.
Maine Natural Health, Inc. is recalling Rejuvenate Natural Dietary Supplement because it fails to declare the allergen milk.
GE Healthcare is recalling 147 Discovery NM 630 nuclear imaging systems to update maintenance procedures and prevent loose fasteners from causing parts to fall on patients.
Champion Bus is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.
Remel Inc is recalling Legionella BCYE Growth Supplement because it may fail to recover Legionella pneumophila, leading to false negative identification.
Steris is recalling 5085 and 5085SRT surgical tables because column shrouds may become damaged, potentially preventing the table from raising or lowering.
Siemens is recalling 164 Artis zeego systems because a cable may be routed incorrectly, potentially causing system failure during procedures.
Jaguar is recalling 2014-2015 XJ vehicles because brake line junctions may leak fluid, potentially reducing braking ability and increasing crash risk.
Health Wise is recalling 12,196 containers of Vanilla Pro-Med. 100 shakes because steel wool was found in the product.
GE Healthcare is recalling 22 Brivo NM615 nuclear imaging systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.
AFX North America is recalling specific FX-76 motorcycle helmets that failed federal impact tests. Riders may face serious injury in a crash.
Maine Natural Health, Inc. is recalling Endurance Daily Vanilla Dietary Supplement because it fails to declare the milk allergen.
Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.
Integra LifeSciences Corp. is recalling 12 units of Reverse Shoulder System cutting templates because the threaded handle was welded backwards, resulting in an incorrect cutting angle.
Raymond-Hadley Corp. is recalling Pride of Africa brand Farina because label review revealed the product contains undeclared wheat.
Maine Natural Health is recalling Endurance Daily Chocolate dietary supplements because they fail to declare milk as an allergen.
Masimo Corporation is recalling specific SET uSpO2 Pulse Oximetry Cables due to crossed internal wires that may cause the monitoring device to display inverted SpO2 values.
Mohawk Industries is recalling Altitude Gold shag rugs sold at The Home Depot because large sizes fail federal flammability standards, posing fire and burn risks.
American Medical Systems is recalling AMS 700 Series Accessory Kits because supplier-supplied Keith needles may bend or break when used with the Furlow tool.
Raymond-Hadley Corp. is recalling Pride of Africa brand Semo Semolina because label review revealed the product contains undeclared wheat.
Latin Specialties, Inc. is recalling Florida avocados distributed in Texas because the product tested positive for Salmonella contamination.
Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.
Maine Natural Health is recalling Pure Whey Chocolate dietary supplements because the labels fail to declare the allergen milk.
Maine Natural Health, Inc. is recalling Daily Balance Natural Dietary Supplement because it fails to declare milk as an allergen.
Publix Bakery Plant is recalling 1,002 cases of Asian Mix clamshells because the product contains peanuts that are not declared on the label.
Mondelez Global LLC is voluntarily recalling Chiclets Gum because the label fails to declare soy lecithin, a common allergen.
Mondelez Global LLC is voluntarily recalling Chiclets Peppermint Gum because the label fails to declare soy lecithin, a common allergen.
Mondelez Global LLC is voluntarily recalling Chiclets Assorted Variety Multipak fruit flavor gum due to undeclared soy lecithin on the label.
Toyota is recalling specific models because seat cushion compression may damage heater wiring, creating a fire and injury risk.
Maine Natural Health, Inc. is recalling Recovery Vanilla dietary supplements because the labels fail to declare milk and shellfish allergens.
Whole Foods Market recalls 365 Organic Raisin Granola because it may contain pecans and coconut not listed on the label.
China Manufacturers Alliance is recalling specific Bluestar trailer tires that may develop sidewall blisters, potentially causing loss of vehicle control.
Maine Natural Health, Inc. is recalling Pure Whey Vanilla dietary supplements because the packaging fails to declare the allergen milk.
Mondelez Global LLC is voluntarily recalling specific packages of Chiclets Fruit Flavor Gum because the label fails to declare soy lecithin.
Hoppe's is recalling Semi-Auto Gun Bore Cleaner bottles because the child-resistant caps can become loose, posing a risk of chemical ingestion.
K. Heeps, Inc. is recalling approximately 2,902 pounds of Bratwurst and Bangers sausage products because they contain undeclared soy lecithin, a known allergen.
Olympus is recalling DS-5500 digital audio recorders because they can overheat while charging, posing a burn hazard to consumers and property.
Maine Natural Health, Inc. is recalling Endurance Pre Race Pina Colada dietary supplements because they fail to declare the milk allergen.
DePuy Orthopaedics is recalling ATTUNE Intuition Distal Femoral Jigs because a pin bushing defect could cause the plastic to fracture or displace during use.
Maine Natural Health, Inc. is recalling Recovery Chocolate dietary supplements because they fail to declare milk and shellfish allergens.
GE Healthcare is recalling 478 nuclear medicine imaging devices because loose fasteners could cause a portion of the system to fall onto a patient during a scan.
Maine Natural Health is recalling Recovery Natural protein supplements because they fail to declare milk and shellfish allergens.
Integra LifeSciences is recalling 60 Licox Pt02 monitors because the USB port may not allow users to extract trend data as described in the manual.
Contract Packaging Resources Inc. is recalling Assured Naproxen Sodium Tablets because correct labeled bottles of Assured Ibuprofen softgels were mistakenly packaged into Naproxen cartons.
GE Healthcare is correcting OEC UroView 2800 systems because prior component revisions may have been incorrectly installed.
Davol, Inc. is recalling 78 units of Bard PerFix Light Plug because the patient record label did not match the actual product in the packaging.
GE Healthcare is recalling five FlexiView 8800 systems because prior component revisions were potentially installed on these units.
Medtronic Vascular is recalling 11 Launcher Coronary Guide Catheters because they have a usable length of 90 cm instead of the labeled 55 cm.
Zimmer, Inc. is recalling 138 units of Persona Stemmed 5 Degree Cemented Tibia knee components due to a cleaning process validation failure.
Fougera Pharmaceuticals is recalling specific lots of Fluocinonide Gel USP, 0.05% because they may not meet USP requirements for residual solvents.
Oro Candy Distributors is recalling Vanilla Cookies (Mantecaditos) because they contain undeclared color additives. Consumers should stop eating the product.
Philips Medical Systems is recalling 708 MX 16-slice CT Scanner Systems because scan images may display left and right sides reversed, potentially leading to misinterpretation of patient position.
GE Healthcare is recalling 26 OEC MiniView 6800 C-Arms because prior component revisions may have been incorrectly installed.
Maquet Cardiovascular is recalling 331 Cardiohelp-I Systems due to a software issue that may display an erroneous 'Battery Needs Service' message after startup.
GE Healthcare is correcting 311 OEC 9800 imaging systems worldwide because prior component revisions may have been incorrectly installed.
Siemens Healthcare Diagnostics is recalling 1,381 units of Rapid Neg BP Combo Panel Type 3 due to an increase in false positive susceptible results.
Fresenius Kabi is recalling Haloperidol Decanoate Injection vials due to an out-of-specification impurity result. The recall covers 216,517 vials distributed nationwide and in Puerto Rico.
CooperSurgical is recalling 17 MILEX Pessary Kits because the packaging displays an incorrect expiration date.
Micro Labs USA Inc. is recalling 1,008 bottles of Simvastatin Tablets, 10 mg, because the product failed impurity content specifications.
Siemens Healthcare Diagnostics is recalling the IMMULITE Calcitonin Control Module due to a typographical error in the expiration date on the instructions for use.
CooperSurgical is recalling 6 units of MILEX Pessary Kits due to incorrect expiration dates printed on the packaging.
Volvo is recalling 2011-2014 VAH and VNL trucks because tires may fail prematurely under specific conditions, increasing crash risk.
Volvo is recalling certain 2012-2015 VHD, VNL, and VNM trucks because the Eco-Roll feature may fail to re-engage the drivetrain, increasing crash risk.
City Line Foods is expanding a recall of 1.2 million pounds of frozen pretzel dog products due to misbranding and undeclared soy lecithin, a known allergen.
Mack is recalling 1,048 model year 2015 CHU and CXU trucks because incorrectly positioned tie rod collars may allow ball sockets to come loose, risking loss of steering.
CoScentrix is recalling approximately 256,000 DD brand candles sold at Hobby Lobby because the high flame can ignite the wax surface, posing a fire hazard.
Isuzu is recalling 3,564 model year 2012-2014 Reach chassis because the brake light switch may bend or corrode, potentially failing to activate brake lights and increasing crash risk.
Black Diamond Inc. is recalling Whippet and Carbon Whippet ski poles because the stainless steel pick can break, posing a risk of injury to users on slopes.
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