Archive
607 recalls were announced in May 2013.
Of the 607 recalls this month scored against our rubric, 4% are Critical, 37% are Severe.
Which agencies issued them
Ford is recalling 2013 Fusion vehicles manufactured in April 2013 because a missing clip in the steering gear could cause loss of steering control.
Ford is recalling 2013 Ford and Lincoln vehicles because a cracked fuel delivery module may leak fuel, creating a fire risk.
Ford is recalling 2013 Lincoln MKZ vehicles equipped with engine block heaters because the cord insulation may crack, exposing wires and increasing the risk of electric shock.
CODA Automotive is recalling 117 model year 2012 CODA vehicles because improperly rolled side curtain airbags may fail to deploy in a crash, increasing injury risk.
Teavana is recalling approximately 445,000 glass tea tumblers in the U.S. and 24,850 in Canada because they can break or shatter unexpectedly, posing laceration and burn hazards.
Fred Meyer is recalling Dan-Dee Chicken Dance Easter Chicks because the toy's music volume exceeds safety standards, posing a hearing damage risk.
Whole Foods Market is recalling Peanut Sesame Noodles distributed in Texas due to potential Salmonella contamination from Sunland, Inc. peanuts.
Brookshire Grocery Company is recalling Goldenbrook Farms Peanut Butter Bash Ice Cream because the peanut butter ingredient may be contaminated with Salmonella.
Go Max Go Foods is recalling Cleo's Peanut Butter Cups because they contain undeclared milk despite being labeled as dairy-free.
Go Max Go Foods is recalling Jokerz vegan candy bars because they contain undeclared milk despite being labeled dairy-free.
Conagra is recalling Orville Redenbacher's Classic Kettle Korn popcorn because it may contain undeclared milk, posing a health hazard to consumers with milk allergies.
Go Max Go Foods is recalling Twilight Candy Bars labeled as dairy-free because they contain undeclared milk.
Whole Foods Market is recalling Chicken Spring Rolls because they were manufactured with peanuts from Sunland, Inc., which may be contaminated with Salmonella.
Go Max Go Foods is recalling Snap! crisped rice bars labeled as dairy-free because they contain undeclared milk.
Krinos Foods is recalling specific lots of Tahini ground sesame seeds due to a risk of Salmonella contamination. Consumers should check expiration dates and stop using affected products.
Lloyd Inc. of Iowa is recalling Levothroid (levothyroxine sodium) tablets due to cGMP deviations and stability failures. The recall covers specific lots distributed nationwide and to Puerto Rico.
Go Max Go Foods is recalling Buccaneer Candy Bars labeled as dairy-free because they contain undeclared milk.
Altec is recalling 2010-2012 aerial devices because a battery cable could short to ground and cause a fire.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab tablets due to cGMP deviations and stability failures. The product was distributed to Forest Laboratories for repackaging.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab 0.175 mg tablets due to cGMP deviations and stability failures. The product was distributed to Forest Laboratories for repackaging.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg and the specific fish species.
Go Max Go Foods is recalling Mahalo Candy Bars labeled as dairy-free because they contain undeclared milk.
Alfred Louie Inc. is recalling 10-pound packages of mung bean sprouts because FDA environmental samples found Listeria monocytogenes in the facility.
Aston Martin is recalling specific 2012-2014 models because a manufacturing error may cause the throttle pedal arm to break, preventing the driver from maintaining or increasing engine speed.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Ball - Shrimp Ball because the label failed to list egg and the fish species.
Go Max Go Foods is recalling Thumbs Up Candy Bars labeled as dairy-free because they contain undeclared milk.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg and the specific fish species.
Lloyd Inc. of Iowa is recalling 5.7 million Thyro-Tab tablets because stability failures in previous lots make it impossible to verify the quality of the current lots.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg as an ingredient and did not declare the species of fish.
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Separation Technology, Inc. is recalling SlidePrep Plus Cytology Centrifuges manufactured before January 1, 2013, because they may start up unexpectedly when exposed to electrostatic discharge.
Roche Diagnostics is recalling software for the cobas e 602 module because it may produce incorrect test results under specific conditions.
Pottery Barn Kids is recalling Sweet Lambie Crib Bumpers because loose stitching can entangle infants. Consumers should stop using affected bumpers and contact the company for a refund or replacement.
Hammary Furniture is recalling about 165 dining side chairs because the leg connections can flex, posing a fall hazard. No injuries have been reported.
Medical Information Technology, Inc. is recalling 56 MEDITECH Bi-Directional interactive Communication Analyzer Interface devices due to incorrect transmission of laboratory results.
Roche Molecular Systems is recalling 425 cobas 4800 systems because rare channel-shift errors may cause test results to be reported in the wrong channel.
Clement Pappas & Co. is recalling Wild Harvest Organic Cranberry Juice because an ingredient contained patulin levels between 57.4 and 100 ppb.
Moller Vital is recalling 1,460 Molift Smart 150 patient lifts because the leg spreading mechanism may fail to hoist and collapse if assembled incorrectly.
Clement Pappas & Co. is recalling Meijier Organics Cranberry Juice because an ingredient contained patulin levels between 57.4 and 100 ppb.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Clement Pappas & Co. is recalling Simple Truth Organic Apple Juice because it contains patulin levels exceeding safety limits.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Brake Parts Inc. is recalling specific Hydro-Max brake master cylinders because the fluid level indicator may fail to warn drivers of low brake fluid, potentially increasing crash risk.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because product coatings require 510K approval.
H&M is reannouncing a recall of children's water bottles because the spouts can break off, posing a choking hazard. Consumers should stop using the bottles and contact H&M for a refund.
Alfred Louie Inc. is recalling 5-pound bags of soy bean sprouts because FDA environmental samples detected Listeria monocytogenes in the facility.
Vive La Fete is recalling specific children's pajama sets because they fail federal flammability standards, posing a burn risk.
Progressive Medical is recalling PTFE coated laparoscopic electrodes because the product coatings require 510K approval.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Moller Vital is recalling 7,555 Molift Smart 150 units because the leg spreading mechanism may fail to hoist and collapse if assembled incorrectly.
Motovan is recalling Zox Old School Motorcycle Helmets (size XL) manufactured in December 2008 because they failed federal impact and penetration safety tests.
KTM North America is recalling about 7,000 KTM and Husaberg motorcycles because a malfunctioning throttle cable can cause an uncontrollable throttle, posing a crash hazard.
Blue Bird is recalling 346 2014 Vision school buses because improperly adjusted brake light switches may delay illumination or remain on, increasing crash risk.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because product coatings require 510K approval.
Clement Pappas & Co. is recalling Full Circle Organic 100% Cranberry Juice Blend because an ingredient contained patulin levels between 57.4 and 100 ppb.
Progressive Medical is recalling PTFE coated laparoscopic electrosurgical electrodes because the product coatings require 510K approval.
King Legacy is recalling Levoxyl (levothyroxine sodium) 175 mcg tablets because they were below specification for potency at the expiry stability point.
Clement Pappas & Co. is recalling Wegmans Organic Apple Juice because it contains patulin levels between 57.4 and 100 ppb.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Lloyd Inc. of Iowa is recalling Levothroid tablets due to cGMP deviations and insufficient stability data. The recall covers 142,103 bottles distributed nationwide and to Puerto Rico.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab 0.125 mg tablets due to cGMP deviations and insufficient stability data.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Cefla Dental Group is recalling 173 MyRay RXDC dental x-ray units because they lack required certification and identification labels.
Clement Pappas & Co. is recalling Giant Eagle Nature's Basket Organic Apple Juice because it contains patulin levels between 57.4 and 100 ppb.
Boston Scientific is recalling the LATITUDE Patient Management System software because a system update caused clinic faxes to display illegible characters instead of required patient information.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab tablets due to cGMP deviations and stability failures. The product was repackaged by Forest Laboratories and distributed nationwide.
Lloyd Inc. of Iowa is recalling Levothroid (levothyroxine sodium) tablets due to cGMP deviations and insufficient stability data.
King Legacy is recalling Levoxyl tablets that were below specification for potency at the expiry stability point.
Lloyd Inc. of Iowa is recalling Levothroid tablets due to cGMP deviations and stability failures in previous lots.
Coloplast is recalling 111 units of Restorelle L prostheses because the packaging contains incorrect Instructions For Use pamphlets.
Lloyd Inc. of Iowa is recalling 7.6 million Thyro-Tab tablets due to cGMP deviations and stability failures. The product was distributed nationwide and to Puerto Rico.
Progressive Medical is recalling PTFE coated disposable electrosurgical electrodes because product coatings require 510K approval.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab 0.088 mg tablets due to cGMP deviations and stability failures. The product was repackaged by Forest Laboratories and distributed nationwide.
Philips is recalling 515 CT systems because they stored the sum of CTDIVol values instead of individual slice values, resulting in incorrect data.
Clement Pappas & Co. is recalling Wild Harvest Organic Apple Juice because it contains patulin levels between 57.4 and 100 ppb.
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Lloyd Inc. of Iowa is recalling 9.5 million Thyro-Tab tablets due to cGMP deviations and insufficient stability data.
Lloyd Inc. of Iowa is recalling Levothroid (levothyroxine sodium) tablets due to cGMP deviations and insufficient stability data.
Lloyd Inc. of Iowa is recalling Levothroid tablets due to cGMP deviations and insufficient stability data. The recall affects 12,156 bottles distributed nationwide and to Puerto Rico.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Clement Pappas & Co. is recalling Giant Eagle Nature's Basket Organic Cranberry Juice because an ingredient contained patulin levels between 57.4 and 100 ppb.
ConMed Linvatec is recalling 267 VP1600 HD Still Capture Systems due to a software anomaly that may cause the device to lock up.
King Legacy is recalling Levoxyl (levothyroxine sodium) tablets because they were below specification for potency at the expiry stability point.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Clement Pappas & Co. is recalling Publix Greenwise Organic Cranberry Flavored Juice Blend because an ingredient contained patulin levels between 57.4 and 100 ppb.
Clement Pappas & Co. is recalling Organic Nature's Promise Organic Cranberry Juice Blend because an ingredient contained patulin levels above the limit.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Clement Pappas & Co. is recalling Heinen's organic 100% Apple Juice because it contains patulin levels above acceptable limits.
Unimed Surgical Products is recalling 120,416 laparoscopic electrode hooks due to changes in PTFE coating materials. The devices were distributed in Missouri, Tennessee, and Pennsylvania.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Progressive Medical Inc is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Clement Pappas & Co. is recalling Full Circle Organic 100% Apple Juice because the apple juice concentrate ingredient contained patulin levels between 57.4 and 100 ppb.
Stryker Howmedica Osteonics is recalling 11 units of Triathlon Femoral Distal Augments due to external packaging label errors, including an incorrect glyph and missing size reference.
Clement Pappas & Co., Inc. is recalling Best Choice Clearly Organic Organic Apple Juice because the apple juice concentrate ingredient contained patulin levels between 57.4 and 100 ppb.
Progressive Medical Inc. is recalling PTFE coated disposable electrosurgical electrodes because the product coatings require 510K approval.
Lloyd Inc. of Iowa is recalling 4,440 bottles of Levothroid 50 mcg tablets due to cGMP deviations and stability failures in previous lots.
Lloyd Inc. of Iowa is recalling specific lots of Levothroid tablets due to stability failures and insufficient data to rule out other affected lots.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
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