Jeni’s Splendid Ice Creams get FDA Warning Letter due to Listeria
For the second time, Listeria contamination is a problem for Jeni’s Splendid Ice Creams’ manufacturers. The first recall of Jeni's Splendid Ice Creams was in 2015 after the bacteria was found in Jeni’s production facility. Jeni’s issued a voluntary recall and was out of business for some time. This recent concern began in January … [Read more...] about Jeni’s Splendid Ice Creams get FDA Warning Letter due to Listeria
Hospira Recalls Lot of Injectable Anesthetic Due to Particulate Contamination
Hospira is recalling one lot of an injectable anesthetic due to contamination with particulate matter, which was identified in a single vial. The voluntary recall affects one lot of 0.25% Bupivacaine Hydrochloride Injection, USP (NDC: 0409-1159-02, Lot 59-064- DK, Expiry 1NOV2017). Hospira, a Pfizer company, learned of the … [Read more...] about Hospira Recalls Lot of Injectable Anesthetic Due to Particulate Contamination
Recall: All Lots of Viapro 375 mg Capsules
EG Labs Voluntary Recall All Viapro 375 mg Capsules. In the second such recall we are reporting on this week, EG Labs, LLC, announced today that it is conducting a nationwide voluntary recall of all lots of Viapro, a supplement sold in 375mg capsules. EG Labs initiated the recall after being informed by the Food and Drug … [Read more...] about Recall: All Lots of Viapro 375 mg Capsules
Response quick on peanut butter
Peanut Butter Are Being Recalled Due To A Contamination. Fort Wayne residents were turning in their peanut butter jars after a voluntary recall because of the possibility of a salmonella outbreak. ConAgra Foods Inc announced Thursday a voluntary recall of jars of Peter Pan and Wal-Mart’s Great Value peanut butter. ConAgra is … [Read more...] about Response quick on peanut butter
Novartis Consumer Health Triaminic Vapor Patch Recall
Triaminic Vapor Patch Nationwide Recall. Novartis Consumer Health announced today it is conducting a nationwide voluntary recall of all Vapor Patch product marketed under the Triaminic brand due to the serious adverse health effects that could result if the product is ingested by the child removing the patch and chewing on … [Read more...] about Novartis Consumer Health Triaminic Vapor Patch Recall
Powerlink System Delivery Catheter Recall
Endologix Recall Its Catheters. Endologix, Inc. today announced that it is voluntarily conducting a limited product recall of selected Powerlink System delivery catheters marketed in the U.S., which are used to deliver the Company's minimally invasive treatment for abdominal aortic aneurysms (AAA). This action does not … [Read more...] about Powerlink System Delivery Catheter Recall
The Food and Drug Administration (FDA) Announces Voluntary Recall of Alcohol-Free Mouthwash Made by Carrington Labs
Carrington Labs Recall Alcohol-Free Mouthwash. Carrington Labs of Irving, Texas, has issued a voluntary recall of Medline labeled alcohol-free mouthwash. As a result of this recall, Medline Industries, Inc. Mundelein, Illinois, is initiating a voluntary recall of Personal Hygiene Admission kits containing the same alcohol-free … [Read more...] about The Food and Drug Administration (FDA) Announces Voluntary Recall of Alcohol-Free Mouthwash Made by Carrington Labs
Three Varieties of Childrens Tylenol Recall
Children’s Tylenol Recall Due To Package May Be Confusing And May Cause Improper Dosing. McNeil Consumer & Specialty Recall Varieties Of Children’s Tylenol. McNeil Consumer & Specialty Pharmaceuticals has voluntarily recalled all lots of three varieties of children's TYLENOL as a result of package information which … [Read more...] about Three Varieties of Childrens Tylenol Recall
Guidant Initiates Voluntary Recall of 3.0mm-Diameter MULTI-LINK VISION Coronary Stent System
MULTI-LINK VISION Coronary Stent System. Guidant CorporatioN, a world leader in the treatment of cardiac and vascular disease, today announced that it has initiated a voluntary recall of certain manufacturing lots of the 3.0 mm diameter MULTI-LINK VISION(TM) Coronary Stent System. The action will affect customers in the United … [Read more...] about Guidant Initiates Voluntary Recall of 3.0mm-Diameter MULTI-LINK VISION Coronary Stent System
