Archive
603 recalls were announced in May 2016.
Of the 603 recalls this month scored against our rubric, 4% are Critical, 18% are Severe.
Which agencies issued them
Iowa Select Herbs LLC is recalling Elderberry Fruit products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Osha Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Organic Cold-Pressed Pomegranate Oil because it is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Black Currant dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Cascara Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Ziziphus supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
North Fish USA is recalling vacuum-packaged salted mackerel because Florida inspectors found the products were not produced under an adequate HACCP plan and were held in unsanitary conditions.
Iowa Select Herbs LLC is recalling Valerian Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Jewel Weed under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Hibiscus Flowers under a consent decree because the products are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Yucca Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Goldenseal Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Alcohol-Free Papaya Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling 7.5 fl. oz. bottles of Cranberry because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 10 bottles of 4 fl. oz. Aloe Vera Juice because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Wormseed products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Cudweed products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Garcinia Fruit products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Grape Seed Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Fenugreek Seed because it is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Green Tea Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Organic Papaya Leaf capsules because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Echinacea Purpurea products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Papaya Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Cyperus Leaf because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Akorn, Inc. is recalling specific batches of PEG-Phen Lubricant Eye Drops because they contain particulate matter. Consumers should stop using the affected products.
VistaPharm is recalling 8,901 cases of Oxycodone Hydrochloride Oral Solution because defective container seals may allow the medication to leak.
Medtronic is recalling 81 Midas Rex Dissecting Tools due to incorrect color coding and attachment references on the labeling.
Biosense Webster is recalling Pentaray NAV High-Density Mapping Catheters to clarify contraindication language regarding patients with prosthetic valves.
Iowa Select Herbs LLC is recalling Bilberry Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Carestream Health is recalling Image Suite V4 systems because a complaint reported that image annotations displayed 'L (Left)' instead of 'R (Right)'.
Iowa Select Herbs LLC is recalling 24 bottles of Yarrow Flowers because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Bitter Melon dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Momordica Leaf under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Oatstraw products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Bryant Ranch Prepack Inc. is recalling venlafaxine hydrochloride extended-release tablets that were incorrectly labeled as immediate-release.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Suma Root because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Fujifilm Medical Systems is recalling 2,062 Smart CR Digital Computed Radiography Systems due to reports of power supply failure.
Iowa Select Herbs LLC is recalling 10 bottles of Acerola Berry (Malpighia) liquid supplement because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Milk Thistle Seed products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Olive Leaf dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling specific lots of Licorice Root because the products are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Schizandra Berry under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Oregano Leaf under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Buchu Leaf under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Dulse Leaf products ordered by a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling alcohol-free cilantro leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Gymnema Sylvestre supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Cold Be Gone products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Nettle Leaf dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Lobelia Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Marshmallow Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Quack Grass dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Raspberry Leaf because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Pygeum Bark products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Radiometer America is recalling TCM CombiM Modules 903-111 because the alarm may sound louder than the pre-set maximum volume.
Mako Surgical Corporation is recalling 10 units of the MAKOplasty Hip Array Kit Laminate 150230 because the product may list two part numbers for the RIO Base Array.
Biosense Webster is recalling Pentaray Catheters to clarify contraindication language regarding patients with prosthetic valves in the product labeling.
Toshiba American Medical Systems is recalling three Celesteion PET/CT systems due to potential degradation of detector performance.
Iowa Select Herbs LLC is recalling Yohimbe Bark products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Medtronic is recalling CareLink and CareLink Express monitors because a firmware update contained incorrect dial-up configuration data, potentially preventing data transmission to the CareLink Network.
A-S Medication Solutions LLC is recalling 2,730 bottles of Acetaminophen & Codeine Phosphate Tablets because the count on the label was incorrect.
Hospira Inc. is recalling 103,600 vials of Quelicin (Succinylcholine Chloride) Injection because the lot number or expiration date may be faded or missing from the primary label.
Iowa Select Herbs LLC is recalling White Peony Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Juniper Berry products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Beet Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Psoralea Seed under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Blood Root dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Sangre De Grado (Rhizoma rhei) because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Muira Puama products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Magnolia Bark because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 26 bottles of Dandelion Leaf due to misbranding, unapproved new drug status, and adulteration under a consent decree.
Iowa Select Herbs LLC is recalling 12 bottles of Alcohol Free Milk Thistle because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling St John's Wart products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Solomon Seal dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
REV Recreation Group is recalling 2016-2017 Holiday Rambler Endeavor motor homes because a framework section may rub against the front passenger-side tire, causing excessive wear and restricted steering.
Turtle Top is recalling 2016 Odyssey transit buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Winnebago is recalling 2016 Forza, Journey, Itasca Solei, and Meridian motorhomes because front sway bar brackets may not fit properly, risking detachment and crashes.
Harley-Davidson is recalling 2014-2016 Dyna Low Rider motorcycles because engine vibrations may damage the ignition switch, causing the engine to shut off while riding.
Garland Ventures is recalling approximately 114,870 pounds of chicken fried rice products due to possible Listeria monocytogenes contamination.
Newmar is recalling 93 Essex, Mountain Aire, and London Aire motorhomes because power steering hoses may fail due to high fluid temperatures, increasing crash risk.
KTM is recalling 2015-2016 1290 Super Adventure motorcycles because a rear shock absorber may leak oil, causing loss of function and increasing crash risk.
Keystone is recalling 2016-2017 Outback trailers because a TV bracket may not be secured, posing an injury risk if the TV falls.
Elpers is recalling 35 trucks equipped with IMT cranes because the valve bank cover may crack and fall off, creating a road hazard.
American Honda is recalling about 3,300 model year 2016 Honda Pioneer 1000 recreational off-highway vehicles because the front door can open unexpectedly, posing a risk of injury.
Bednest is recalling bedside infant sleepers manufactured after July 2014 because they fail to meet federal safety requirements, posing a fall hazard to babies.
Cybex International is recalling approximately 400 decline free weight benches because the frame can collapse forward, posing an impact injury hazard.
Spartan Motors is recalling 89 Utilimaster Aeromaster vehicles because a wiring defect may leave the lift gate system powered, posing an injury risk to maintenance personnel.
Legacy Beef, LLC is recalling approximately 497 pounds of beef jerky products due to under-processing and potential bacterial pathogens. No illnesses have been reported.
La Autentica Foods is recalling approximately 117,350 pounds of meat tamale products due to possible Listeria monocytogenes contamination. The products were distributed to retail and restaurant locations in Florida and New Jersey.
Chrysler is recalling 2009-2016 Dodge Journey vehicles because the power steering return hose may rupture in cold weather, causing loss of steering assist.
Land Rover is recalling 2015-2016 Discovery Sport vehicles because the license plate illumination lamp may fall out, making the vehicle difficult to identify at night.
Pilgrim's Pride is recalling approximately 5.2 million pounds of fully cooked chicken products that may be contaminated with extraneous metal materials.
The Grey Plume Provisions, LLC is recalling approximately 471 pounds of charcuterie meat products produced without federal inspection. The products were distributed in Iowa and Nebraska.
General Motors is recalling specific 2016 Chevrolet Malibus because a memory chip failure may cause the loss of anti-lock brakes and electronic stability control, increasing crash risk.
BRP is recalling about 10,600 model year 2013 Can-Am Commander side-by-side vehicles because a steering defect can cause loss of control and crashes.
Munchkin is recalling Latch lightweight pacifiers and clips because the clip cover can detach, posing a choking hazard to young children.
Texas Star Nut and Food Co. is recalling Nature's Eats Almond & Pistachio Duo due to potential Salmonella contamination.
Marathon Ventures Inc. is recalling macadamia nuts under seven brands because FDA testing found Salmonella in a retail package.
Progressive Gourmet Inc. is recalling frozen Edamame Rangoon cartons because they contain undeclared crabmeat, a major allergen.
Looking for a different month? Back to 2016.