Baby Trend Recalls Tango Mini Strollers Due to Fall Hazard
Both of the stroller’s hinge joints can release and collapse under pressure, posing a fall hazard to children in the stroller.
Source: Recall List
Entries by Heather Davis
The Thompson’s Company Recalls Aerosol Waterproofing Wood and Masonry Protectors Due to Fire Hazard
The contents of the cans can react with the package, causing rust to form along the can seam, which could spread to other areas of the can and create pinhole leaks. Leaking propellant poses a fire hazard when it comes into contact with sources of...
Source: Recall List
Lipari Foods Issues Recall of Various Wedge Deli Sandwiches Due to Potential Contamination of Listeria Monocytogenes
Lipari Foods has issued a voluntary recall of various Premo and Fresh Grab wedge sandwiches due to potential contamination of Listeria monocytogenes.
Source: Food and Drugs Administration--Recalls/Safety Alerts
Lipari Foods Issues Voluntary Recall Expansion on Additional Sandwiches Due to Potential Contamination of Listeria Monocytogenes
Lipari Foods has issued a voluntary recall expansion of additional Premo and Fresh Grab sandwiches due to potential contamination of Listeria monocytogenes.
Source: Food and Drugs Administration--Recalls/Safety Alerts
Denton Pharma, Inc. dba Northwind Pharmaceuticals Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity
Denton Pharma, Inc. dba Northwind Pharmaceuticals, an affiliate of Northwind Pharmaceuticals, LLC (“Northwind”) today announced the voluntary recall of all unexpired lots of Ranitidine Tablets, 150 mg and 300mg, to the consumer level. The recall is in ...
Source: Food and Drugs Administration--Recalls/Safety Alerts
Taro Pharmaceuticals U.S.A., Inc. Issues Voluntary Nationwide Recall of Lamotrigine Tablets USP, 100 mg, 100 Count Bottles
Taro Pharmaceuticals U.S.A., Inc. (“Taro” or the “Company”) is voluntarily recalling one (1) lot of Lamotrigine 100 mg Tablets, Lot # 331771 (expiration date June 2021) in 100 count bottles, NDC 51672-4131-1 to the consumer level.
Source: Food and Drugs Administration--Recalls/Safety Alerts
Stryker Launches Voluntary Field Action for Specific Units of The LIFEPAK® 15 Monitor/Defibrillator
Stryker announced today that the company is launching a voluntary field action on specific units of the LIFEPAK 15 monitor/defibrillators.
Source: Food and Drugs Administration--Recalls/Safety Alerts
Libbey Glass Recalls Milk Bottles Due to Laceration Hazard
The bottles can break unexpectedly during use, posing a laceration hazard.
Source: Recall List
Thesaurus Global Marketing Recalls Tricycles Due to Violation of the Federal Lead Paint Ban; Risk of Poisoning; Sold Exclusively at Amazon.com (Recall Alert)
Paint on the canopy’s frame contains levels of lead that exceed the federal lead paint ban and tricycle components contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse ...
Source: Recall List
Boston Warehouse Trading Corp. Recalls Holiday Travel Mugs Due to Fire Hazard; Sold Exclusively at Meijer Stores
The mugs are mislabeled as microwave safe. If microwaved, the metallic print on the mug can spark, posing a fire hazard.
Source: Recall List
