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Trader Joe's - Your Neighborhood Grocery Store

Trader Joe's - Your Neighborhood Grocery Store : Trader Joe's -    To Our Valued Customers: We have been alerted by our supplier of  Trader Joe’s Organic Tropical Fruit Blend  (SKU# 51191) that product with  BEST BY  dates of  04/25/24, 05/12/24, 05/23/24, 05/30/24,  and  06/07/24  may have the potential to be contaminated with Hepatitis A. No illnesses have been reported to date, and all potentially affected product has been removed from sale and destroyed. If you purchased any Organic Tropical Fruit Blend, please do not eat it. We urge you to discard the product or return it to any Trader Joe’s for a full refund. Customers with questions may contact Trader Joe’s Customer Relations at  (626) 599-3817  [Monday through Friday, 6:00 am to 6:00 pm Pacific Time] or  send us an email . We sincerely apologize for the inconvenience.

Recalled AirWick air fresheners pose laceration hazard

Recalled AirWick air fresheners pose laceration hazard : The products were sold in 8-ounce aerosol cans in “Fresh Linen” scent (blue and white can, white cap, green Airwick logo, UPC 0-62338-74734-7) and “Fresh Waters” scent (green and white can, white cap, green Airwick logo, UPC 0-62338-77002-4) with batch code B22077-NJ and date code 18/03/22.

Proper Trade LLC/My Stellar Lifestyle Issues Voluntary Nationwide Recall of Wonder Pill Capsules Due to the Presence of Undeclared Tadalafil | FDA

Proper Trade LLC/My Stellar Lifestyle Issues Voluntary Nationwide Recall of Wonder Pill Capsules Due to the Presence of Undeclared Tadalafil | FDA

Salon Technologies, Inc. Issues Voluntary Nationwide Recall of Antica Ocean Citron Hand Sanitizer ( Alcohol ) Gel 65% Due to the Presence of Benzene | FDA

Salon Technologies, Inc. Issues Voluntary Nationwide Recall of Antica Ocean Citron Hand Sanitizer ( Alcohol ) Gel 65% Due to the Presence of Benzene | FDA

FSIS Issues Public Health Alert For Chicken Entree Products Due To Misbranding And An Undeclared Allergen | Food Safety and Inspection Service

FSIS Issues Public Health Alert For Chicken Entree Products Due To Misbranding And An Undeclared Allergen | Food Safety and Inspection Service

Banana Boat recalls sunscreen spray, citing carcinogenic chemical in product : NPR

Banana Boat recalls sunscreen spray, citing carcinogenic chemical in product : NPR : The maker of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 said trace amounts of the cancer-causing chemical benzene were found in the propellant that sprays the product from the can.

SunVilla Solar Patio Umbrellas Sold At Costco Recalled After Multiple Fires – CBS Sacramento

SunVilla Solar Patio Umbrellas Sold At Costco Recalled After Multiple Fires – CBS Sacramento : Solar-powered patio umbrellas sold exclusively at Costco have been recalled in the United States and Canada after some umbrellas caught fire, authorities said.

More than 400,000 bottles of over-the-counter medication recalled due to issues with child-proofing | The Hill

More than 400,000 bottles of over-the-counter medication recalled due to issues with child-proofing | The Hill : The Consumer Product Safety Commission on Thursday announced the recall of over 400,000 bottles of over-the-counter medicine due to issues with the child-resistant packaging, which did not meet the requirements in the Poison Prevention Packaging Act. Aurohealth recalled about 137,300 units of Walgreens brand acetaminophen, as well as approximately 25,660 units of Kroger brand arthritis…

Buzzagogo, Inc. Issues Voluntary Nationwide Recall of Allergy Bee Gone for Kids Nasal Swab Remedy Due to Potential Microbial Contamination | FDA

Buzzagogo, Inc. Issues Voluntary Nationwide Recall of Allergy Bee Gone for Kids Nasal Swab Remedy Due to Potential Microbial Contamination | FDA

Leonard Novelty Bakery Announced a Recall Involving Carrot Cake Squares Due to Undeclared Walnuts | FDA

Leonard Novelty Bakery Announced a Recall Involving Carrot Cake Squares Due to Undeclared Walnuts | FDA

FDA: Strawberries Recalled As Hepatitis A Virus Outbreak Has Left 16 Hospitalized

FDA: Strawberries Recalled As Hepatitis A Virus Outbreak Has Left 16 Hospitalized : The outbreak has already left at least 17 people infected and 12 hospitalized in the U.S. and at least 10 infected and four hospitalized in Canada.

Indiana Botanic Gardens, Inc. Issues Allergy Alert on Undeclared Peanuts in Prune & Senna Softgels | FDA

Indiana Botanic Gardens, Inc. Issues Allergy Alert on Undeclared Peanuts in Prune & Senna Softgels | FDA : Indiana Botanic Gardens Inc. of Indiana, is recalling its 30-count bottles of Botanic Choice brand Prune & Senna Softgels because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. Th

Henkel Corp. Voluntarily Recalls Alterna® Bond Repair Leave-in Heat Protection Spray Due to Possible Health Risk | FDA

Henkel Corp. Voluntarily Recalls Alterna® Bond Repair Leave-in Heat Protection Spray Due to Possible Health Risk | FDA

Disney hand sanitizers recalled; benzene, methanol detected

Disney hand sanitizers recalled; benzene, methanol detected

Fitbit Recalls Ionic Smartwatches Due to Burn Hazard; One Million Sold in the U.S. | CPSC.gov

Fitbit Recalls Ionic Smartwatches Due to Burn Hazard; One Million Sold in the U.S. | CPSC.gov

TCP HOT Acquisition LLC dba HRB Brands Issues Voluntary Nationwide Recall of Sure and Brut Aerosol Sprays Due to the Presence of Benzene | FDA

TCP HOT Acquisition LLC dba HRB Brands Issues Voluntary Nationwide Recall of Sure and Brut Aerosol Sprays Due to the Presence of Benzene | FDA

Your Favorite Shop Issues Voluntary Nationwide Recall of the Red Pill Capsules, Due to the Presence of Undeclared Tadalafil | FDA

Your Favorite Shop Issues Voluntary Nationwide Recall of the Red Pill Capsules, Due to the Presence of Undeclared Tadalafil | FDA

FDA Alert: AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Polymyxin B for Injection USP, 500,000 Unit per Vial, Due to the Presence of Particulate Matter

FDA Alert: AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Polymyxin B for Injection USP, 500,000 Unit per Vial, Due to the Presence of Particulate Matter

Lohxa LLC Issues Voluntary Nationwide Recall of Senna Syrup 8.8mg/5mL Due to Microbial Contamination | FDA

Lohxa LLC Issues Voluntary Nationwide Recall of Senna Syrup 8.8mg/5mL Due to Microbial Contamination | FDA

Covidien, LP Recalls Puritan Bennett 980 Series Ventilator Due to Manufacturing Assembly Error | FDA

Covidien, LP Recalls Puritan Bennett 980 Series Ventilator Due to Manufacturing Assembly Error | FDA : Covidien, LP (part of Medtronic) is recalling its Puritan Bennett 980 Series Ventilator due to a capacitor manufacturing assembly error.