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)
/in Consumer Product Safety Commission/by Heather DavisPaint 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 health issues.
Source: Recall List
Boston Warehouse Trading Corp. Recalls Holiday Travel Mugs Due to Fire Hazard; Sold Exclusively at Meijer Stores
/in Consumer Product Safety Commission/by Heather DavisThe mugs are mislabeled as microwave safe. If microwaved, the metallic print on the mug can spark, posing a fire hazard.
Source: Recall List
Mavidon Issues Voluntary Worldwide Recall of Manufactured Products Including Lemonprep® Tubes And Single Use Cups Pediaprep® Tubes And Single Use Cups Wave Prep® Tubes And Single Use Cups Cardio Prep Single Use Cups Due To Burkholderia Cepacia Contamination
/in Recalls from FDA/by Heather DavisMavidon is voluntarily recalling all lots of products manufactured at our facility including LemonPrep®, PediaPrep® and Wave Prep 4-ounce tubes and single use cups, Cardio Prep and Collodions, Collodion removers due to contamination with Burkholderia cepacia.
Source: Food and Drugs Administration--Recalls/Safety Alerts
Fresh Location Announces Product Recall Due to Possible Listeria Contamination
/in Recalls from FDA/by Heather DavisProtein Snack Tray 6.44 oz total weight packaged in a 4-compartment plastic tray with UPC: 8-5511000804-6 and with Fresh by lot dates of: 12/21/19, 12/22/19, 12/24/19, 12/27/19, 12/28/19, 12/29/19, 12/31/19, 01/03/20, 01/04/20. Protein Trail Mix 3.52 oz total weight packaged in a 10.5 ounce pla
Source: Food and Drugs Administration--Recalls/Safety Alerts
Mylan Initiates Voluntary Nationwide Recall of Three Lots of Nizatidine Capsules, USP, Due to the Detection of Trace Amounts of NDMA (N-Nitrosodimethylamine) Impurity Found in the Active Pharmaceutical Ingredient Manufactured by Solara Active Pharma Sciences Limited
/in Recalls from FDA/by Heather DavisMylan N.V. (NASDAQ: MYL) today announced that its U.S. based Mylan Pharmaceuticals business is conducting a voluntary nationwide recall, to the consumer level, of three lots of Nizatidine Capsules, USP (including the 150mg and 300mg strengths). While Mylan has not received any reports of adverse eve
Source: Food and Drugs Administration--Recalls/Safety Alerts
Appco Pharma LLC Issues Voluntary Nationwide Recall of Ranitidine Hydrochloride Capsules 150 mg and 300 mg Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA)
/in Recalls from FDA/by Heather DavisAppco Pharma LLC (Appco) is voluntarily recalling all quantities and lots, within expiry, of Ranitidine Hydrochloride Capsules to the Consumer level. Ranitidine Hydrochloride Capsules are being recalled because of the presence or potential presence of N-nitrosodimethylamine (NDMA)
Source: Food and Drugs Administration--Recalls/Safety Alerts
Jeni’s Splendid Ice Creams Issues Voluntary Recall of Cold Brew with Coconut Cream
/in Recalls from FDA/by Heather DavisJeni’s Splendid Ice Creams has initiated a voluntary recall of three batches of Cold Brew with Coconut Cream Non-Dairy Frozen Dessert pints because they may contain an undeclared milk allergen
Source: Food and Drugs Administration--Recalls/Safety Alerts
Purely Elizabeth Recalls Pouches of Chocolate Sea Salt Probiotic Granola Recall Due to a Mislabeling Error That Has Resulted in an Undeclared Allergen
/in Recalls from FDA/by Heather DavisPurely Elizabeth is initiating a voluntary recall of their Chocolate Sea Salt Probiotic granola due to a mislabeling error that has resulted in an undeclared allergen (walnuts) being present.
Source: Food and Drugs Administration--Recalls/Safety Alerts
Ducktrap River of Maine Recalls One Lot of Herring Center Cuts in Wine Sauce Due to Undeclared Dairy in Product
/in Recalls from FDA/by Heather DavisDucktrap River of Maine of Belfast, Maine is announcing a voluntary recall of Herring Center Cuts in Wine Sauce identified with sell by date Jul 29, 2020 because these products contain undeclared milk due to an incorrect label.
Source: Food and Drugs Administration--Recalls/Safety Alerts
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