Tandem Diabetes Care, Inc. Recalls Version 2.7 of the Apple iOS t:connect Mobile App Used in Conjunction with t:slim X2 Insulin Pump with Control-IQ Technology Prompted by a Software Problem Leading to Pump Battery Depletion

Please be aware, this recall is a correction, not a product removal. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Names: Version 2.7 of the Apple iOS t:connect mobile app used in conjunction with…

Palmer Candy Company Recalls White Confectionary Products Because of Possible Health Risk

Summary Company Announcement Date: May 05, 2024 FDA Publish Date: May 06, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Salmonella Company Name: Palmer Candy Company Brand Name: Brand Name(s) Freshness Guaranteed, Palmer, Sweet Smiles, Snackin’ With The Crew, Casey’s, Sconza Chocolates, Favorite Day…

Recall_Supplier Recalls Impact Two Hy-Vee Products Third-Party Manufacturers Alert Retailer of Potential for Contamination; No Illnesses Reported

Summary Company Announcement Date: May 06, 2024 FDA Publish Date: May 06, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Salmonella Company Name: Hy-Vee Inc Brand Name: Brand Name(s) Product Description: Product Description Plain Whipped Cream Cheese, Plain Cream Cheese, and Cookies & Cream…

Hormel Foods Sales, LLC Recalls a Limited Number of Planters® Honey Roasted Peanuts 4 Oz. and Planters® Deluxe Lightly Salted Mixed Nuts 8.75 Oz. Because of Possible Health Risk

Summary Company Announcement Date: May 03, 2024 FDA Publish Date: May 03, 2024 Product Type: Food & Beverages Nuts & Nut Products Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: Hormel Foods Sales, LLC Brand Name: Brand Name(s) Product Description: Product Description Honey Roasted Peanuts and…

Chuao Chocolatier Recalls Its: .39 oz /11 Gram Potato Chip Mini Bar Lot 4022 Due to Undeclared Hazelnuts

Summary Company Announcement Date: May 03, 2024 FDA Publish Date: May 03, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Hazelnuts Company Name: Chuao Chocolatier Brand Name: Brand Name(s) Chuao Chocolatier Product Description: Product Description Potato Chip Mini Chocolate Bar Company Announcement FOR IMMEDIATE RELEASE – May 3, 2024,…

Opioid Manufacturer Endo Health Solutions Inc. Ordered to Pay $1.536B In Criminal Fines and Forfeiture for Distributing Misbranded Opioid Medication

Department of JusticeUS Attorney’s OfficeOffice of Public Affairs For Immediate ReleaseFriday, May 3, 2024 Endo Health Solutions Inc. (EHSI) was ordered today to pay $1.086 billion in criminal fines and an additional $450 million in criminal forfeiture — the second-largest set of criminal financial penalties ever levied against a pharmaceutical company —for violations of the…

STOP CLOPEZ CORP Issues Voluntary Worldwide Recall of Schwinnng Capsules Due to the Presence of Undeclared Nortadalafil

Summary Company Announcement Date: April 22, 2024 FDA Publish Date: April 23, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Product is tainted with Nortadalafil Company Name: STOP CLOPEZ CORP Brand Name: Brand Name(s) Product Description: Product Description Herbal Dietary Supplement Company Announcement FOR IMMEDIATE RELEASE – 04/22/2024– Hollywood, FL, US, STOP CLOPEZ…

Biloxi City Councilman Pleads Guilty to Drug Conspiracy Involving Vape Shops

Department of JusticeU.S. Attorney’s OfficeSouthern District of Mississippi For Immediate ReleaseThursday, May 2, 2024 Gulfport, Mississippi – A Biloxi City Councilman pleaded guilty to conspiracy to possess with intent to distribute a Schedule I controlled substance. Robert Leon Deming, III, 47, pled guilty in U.S. District Court in Gulfport.   According to court documents and…

SonarMed Inc. Recalls Airway Monitors Due to a Software Anomaly Resulting in Failure to Detect a Partial Obstruction in 2.5mm Sensors and Up To 3mm Distal to the Sensor Tip

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.  Recalled Product  Product Names: SonarMed Airway monitors  Product Codes: OQU  Model Numbers: AW-M0001 Distribution Dates: October 13, 2022 to October 6, 2023 Devices Recalled in the U.S.: 145 Date…