Recent FDA & US Consumer Product Safety Commission Recalls
Currently Showing FDA & CPSC Recall Notices
Note: Updates automatically every five minutes
WilliamsRDM Recalls StoveTop FireStop Microhood Due to Safety Hazard (Recall Alert)
Filed: Thursday,August 21, 2014, 6:00 am
The Microhood's front canister can fall from the unit and fail to suppress the fire.
SolarWorld Recalls Solar Systems with Copper Grounding Lugs Due to Electrocution, Electric Shock or Fire Hazard
Filed: Thursday,August 21, 2014, 3:00 am
The bare-copper grounding lugs installed with SolarWorld Solar Systems can corrode, resulting in a faulty ground circuit. This poses a risk of shock, electrocution and fire.
CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
Filed: Wednesday,August 20, 2014, 8:36 am
On July 10, 2014, Cook Medical initiated a recall of 696 of its CloverSnare™ 4-Loop Vascular Retrieval Snare devices. The device was recalled because of a potential for the loop to separate from the shaft, resulting in loss of device function, potential for embolization of snare fragments and the potential need for intervention to retrieve the separated snare.
Attwood Recalls Kayak and Watersports Storage Hanger Due to Injury Hazard
Filed: Wednesday,August 20, 2014, 3:00 am
The adjustment buckles can release unexpectedly, causing the stored item to fall and injure people nearby.
nSPIRED Natural Foods, Inc. Voluntarily Recalls Certain Retail Lots Of Arrowhead Mills® Peanut Butters, Maranatha® Almond Butters And Peanut Butters And Specific Private Label Nut Butters Because Of Possible Health Risk
Filed: Tuesday,August 19, 2014, 11:32 am
nSpired Natural Foods, Inc. is voluntarily recalling certain retail lots of Arrowhead Mills® Peanut Butters, MaraNatha® Almond Butters and Peanut Butters and specific private label nut butters (listed below) packaged in glass and plastic jars because they have the potential to be contaminated with Salmonella.
Golden Artist Colors Recalls QoR Synthetic Ox Gall due to Skin Irritation (Recall Alert)
Filed: Tuesday,August 19, 2014, 7:00 am
Consumers could experience an allergic skin reaction after long periods of skin contact.
Bexco Recalls Franklin & Ben Mason 4-in-1 Convertible Cribs Due to Fall and Entrapment Hazards
Filed: Tuesday,August 19, 2014, 3:00 am
The side panels on the Franklin & Ben Mason style cribs can separate and create a hazardous gap. This poses a fall hazard and risk of entrapment.
BRITA Recalls Children’s Water Bottles Due to Laceration Hazard
Filed: Tuesday,August 19, 2014, 12:00 am
Children's cartoon character water bottle lid can break into sharp pieces, posing a laceration hazard.
Voluntary Recall Notice of McCormick Ground Oregano Due to Possible Salmonella Risk
Filed: Thursday,August 14, 2014, 1:04 pm
McCormick & Company, Incorporated is initiating a voluntary recall of McCormick® Ground Oregano, 0.75 oz bottle, UPC 0-523561-6 with code dates BEST BY AUG 21 16 H and AUG 22 16 H due to possible contamination with Salmonella. This recall does not impact any other McCormick Ground, Whole or Oregano Leaves products.
Snowmobiles Recalled by Arctic Cat Due to Fuel Leak and Fire Hazard (Recall Alert)
Filed: Thursday,August 14, 2014, 7:00 am
Fuel can leak from the Arctic Cat XF 7000 and ZR 7000 snowmobiles' fuel line assembly, posing a fire hazard to riders.
Amgen Issues Voluntary Recall of AranespÂ® (darbepoetin alfa) (500 mcg) Prefilled Syringes in Several Countries Outside of the United States Due to the Presence of Visible Particulates
Filed: Thursday,August 14, 2014, 6:59 am
Amgen (NASDAQ:AMGN) initiated a voluntary recall on June 26, 2014 for nine packaged lots of AranespÂ® (darbepoetin alfa) (500 mcg) prefilled syringes from non-U.S. distributors, wholesalers and a number of hospital pharmacies due to the potential presence of cellulose and/or polyester particles observed in a small number of syringes during a routine quality examination. Lots 1042847, 1044141A, 1044141C, 1044141D, 1046891A, 1046891B, 1047394A, 1047622A, and 1047996A are being recalled as a precautionary measure.
Baxter Voluntarily Initiates U.S. Recall of Two Lots of Peritoneal Dialysis Solution Due to Presence of Particulate Matter
Filed: Thursday,August 14, 2014, 6:54 am
Baxter International Inc. announced today it is voluntarily initiating a recall in the United States of two lots of DIANEAL Low Calcium (2.5mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose 5000mL (Ambu-Flex II) to the hospital/user level. The recall is being initiated due to the presence of oxidized stainless steel, garment fiber, and PVC particulate matter identified during the manufacturing process.
Vornado Air Recalls Electric Space Heaters Due to Fire and Burn Hazards
Filed: Thursday,August 14, 2014, 2:00 am
The Whole Room Vortex heater, model VH110, can overheat and cause the units to melt, catch fire and ignite nearby items.
Baxter Initiates Voluntary Recall of One Lot of 0.9% Sodium Chloride Injection, USP Intravenous (IV) Solution
Filed: Wednesday,August 13, 2014, 10:37 am
Baxter International Inc. announced today it is voluntarily recalling one lot of 0.9% Sodium Chloride Injection, USP 1000 mL, a portion of which was released to customers. The recall is being initiated as a result of particulate matter found near the administration port.
ESL, Interlogix Hard-Wired Smoke Alarms Recalled Due to Failure to Alert Consumers of a Fire
Filed: Wednesday,August 13, 2014, 2:00 am
Radio frequency interference can cause the smoke detectors to fail.
Sunfood Recalls Organic Carob Powder Because Of Possible Health Risk
Filed: Tuesday,August 12, 2014, 5:16 pm
Sunfood of El Cajon, CA is recalling Organic Carob Powder, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
JPC Equestrian Recalls Stirrup Leathers Due to Fall Hazard
Filed: Tuesday,August 12, 2014, 7:30 am
The Henri De Rivel pre-stretched, 48-inch and 54-inch stirrup leathers can crack and break while in use. This poses a fall hazard to the rider.
CoScentrix Recalls Candles in Metal Tins Due to Fire Hazard; Sold Exclusively at Hobby Lobby
Filed: Tuesday,August 12, 2014, 3:00 am
High flames from the “DD” brand CoScentrix candles can ignite the surface wax and the polymer coating on the tin-plated container. This poses a fire hazard.
Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Nine Lots of CUBICIN (daptomycin for injection) 500 mg in 10 mL single use vials Following Complaints of Foreign Particulate Matter in Reconstituted Vials
Filed: Saturday,August 9, 2014, 5:51 am
Cubist Pharmaceuticals, Inc. (NASDAQ: CBST) today announced it is voluntarily recalling nine lots of CUBICIN (daptomycin for injection) to the user level following complaints of foreign particulate matter in reconstituted vials. The administration of particulate matter, if present in an intravenous drug, poses a potential safety risk to patients such as a thromboembolism or a life-threatening pulmonary embolism.
Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegenESlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk
Filed: Thursday,August 7, 2014, 4:55 pm
Regeneca Worldwide a division of VivaCeuticals, Inc. Las Vegas, NV is conducting a voluntary nationwide recall of its RegenESlim appetite control dietary supplement from lot # EX0616R15814 and lot #11414RE5516 because FDA analysis confirmed the presence of DMAA. DMAA is also known as 1,3-dimethylamylamine, methylhexanamine, or geranium extract. DMAA is commonly used as a stimulant, pre-workout, and weight loss ingredient in dietary supplement products. The Food and Drug Administration (FDA) has warned that DMAA is potentially dangerous to health as it can narrow blood vessels and arteries, which can cause a rise in blood pressure or other cardiovascular problems such as shortness of breath, arrhythmias, tightening in the chest, and heart attack.
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