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U.S. Consumer Product Safety Commission
ZLP Manufacturing Recalls Hornet Zip Line Trolleys Due to Fall Hazard (Recall Alert)
The retaining pin can release and cause the two side plates of the trolley to separate and fall off the zip line.
Tektro USA and TRP Recall Bicycle Mechanical Disc Brake Calipers Due to Crash Hazard
The Spyre and Spyre SLC calipers were sold as original and aftermarket equipment on bicycles.
Design Ideas Recalls Magnets Due to Risk of Ingestion
The small magnet can easily detach from the office and refrigerator magnets. If swallowed, the magnets can link together inside the intestines and can cause perforations, sepsis and death.
Canon Recalls to Repair PowerShot SX50 HS Digital Cameras
Canon has received one report of itching and two reports of eye redness and pain.
Air Movers Recalled by Packaging Tape Inc. Due to Fire Hazard
The motor on the recalled CleanFreak air mover/blowers can overheat. The products are used to dry floors in commercial and residential buildings.
Fitness Anywhere Recalls TRX Dip and Hammer Bars Due to Risk of Injury (Recall Alert)
The bar welds on the TRX model exercise machine can break.
Hitachi Koki Recalls Grass Trimmers Due to Fire and Burn Hazards
The gasoline-powered Hitachi and Tanaka-brand grass trimmers can overheat.
Twin-Star Recalls Duraflame Electric Space Heaters Due to Fire and Burn Hazards
The fireplace-looking space heater can overheat, melt, catch fire and ignite nearby items. Property damage reported.
Rowe Fine Furniture Recalls Ottomans Due to Risk of Suffocation (Recall Alert)
Young children can become trapped inside the ottoman's storage compartment.
Mammut Recalls Crevasse Rescue Devices Due to Risk of Injury
The pull cord lock cam on the mountain climbing rescue devices can fail.
National Highway Transportation Safety Administration
HONDA ( 14V056000 )
Dated: FEB 13, 2014 Honda is recalling certain model year 2013 CB500 (FA, F, XA, X) and CBR500 (RA, R) motorcycles. The rocker arm shaft retaining bolts may have been manufactured incorrectly resulting in the bolts loos...
U.S. Food and Drug Administration
Hong Lee Trading Inc. Issues an Alert on Undeclared Sulfites in “Mut Dua Non” Young Coconut Candy (Strips)
Hong Lee Trading Inc., at 225 Johnson Avenue, Brooklyn, NY 11206 is recalling “Mut Dua Non” Young Coconut Candy (Strips) because it contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
Net Food Brand Turkey Dried Apricots Recalled Because of Undeclared Sulfites
Net Foods Import & Export at 711 2nd Street, Secaucus, NJ 07094 is recalling Net Food Brand Turkey Diced Apricots because they contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life threatening allergic reactions if the consume this product.
Pfizer Initiates Nationwide Voluntary Recall of Two Lots of Pfizer’s Effexor XR® 150 Mg Extended-Release Capsules and One Lot of Greenstone’s Venlafaxine HCl 150 Mg Extended-Release Capsules Due to the Possible Presence of Tikosyn® Capsules
Pfizer Inc. is voluntarily recalling one lot of 30-count Effexor XR® (venlafaxine HCl) 150 mg extended-release capsules, one lot of 90-count Effexor XR (venlafaxine HCl) 150 mg extended-release capsules and one lot of 90-count Greenstone LLC-branded Venlafaxine HC1 150 mg extended-release capsules.
Crown Food Distributors, Inc. Issues Allergy Alert on Undeclared Sulfites and Undeclared Yellow #6 in Golden Natural Fruit Island
Crown Food Distributors, Inc. of North Bergen, NJ is recalling 25 oz. large round plastic containers of “Golden Natural Fruit Island” because they contain undeclared sulfites and undeclared FD & C yellow #6. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products.
Gretchen’s Shoebox Express Issues Allergy Alert for Limited Number of Greek Yogurt Raspberry & Lemon Parfait cups Due to Undeclared Eggs.
Out of the utmost caution and care for our customers, Gretchen’s Shoebox Express in Seattle, Washington, is initiating a voluntary recall of a limited number of Greek Yogurt Raspberry & Lemon Parfait cups sold under the Starbucks brand in Seattle and Portland regional Starbucks stores because the product was mislabeled and failed to declare the presence of eggs, an allergen.
Baxter Initiates U.S. Voluntary Recall of One Lot of Peritoneal Dialysis Solution Due to Container-Closure Non-Integrity
Baxter International Inc. announced today it has initiated a voluntary recall in the United States of a single lot of DIANEAL PD-2 Peritoneal Dialysis Solution with 1.5% Dextrose 6000mL (Ambu-Flex II) to the hospital/user level. The recall is being initiated as a result of complaints of particulate matter, identified as mold, resulting from a leak in the container.
House of Flavors Issues Voluntary Recall Due to Possible Undeclared Nut Allergen in Belmont Chocolate Chip Cookie Dough Ice Cream
March 5, 2014 - Ludington, Michigan – House of Flavors Ice Cream Company, based in Ludington, Michigan, is recalling its Belmont Chocolate Chip Cookie Dough Ice Cream because it's ingredients may include an undeclared nut allergen. Consumers who may have an allergy or severe sensitivity to nuts run the risk of serious or life-threatening allergic reaction if they consume this product.
HC Schau and Sons issues allergy alert on undeclared Pine Nuts in ‘Fresh To Go’ Tuscan Style Combo on Tomato Basil Bread (sandwich).
HC Schau and Son of Woodridge Illinois is recalling 3422 individual 8oz units of ‘Fresh To Go Tuscan Style Combo on Tomato Basil Bread’ because it may contain undeclared Pine Nuts (tree nuts).
Plum Organics Voluntarily Recalls Limited Quantity of Two Varieties of World Baby Pouch Products
Plum Organics is voluntarily recalling a limited quantity of two varieties of its World Baby line of pouch products due to intermittent damage to the plastic spouts during manufacturing.
Thoratec Corporation Issues Worldwide Urgent Medical Device Correction Letter to Update its Labeling Regarding the Use of the HeartMate II® LVAS Pocket System Controller
On March 4, 2014, Thoratec Corporation initiated a voluntary worldwide Medical Device Correction in order to update its labeling and training materials for the HeartMate II® LVAS Pocket System Controller (the “Pocket Controller”).
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