[6-14-2024] The Food and Drug Administration is advising consumers not to purchase or use Umary, a product promoted and sold for pain on various websites, including https://www.solovital.com and possibly in some retail stores. FDA laboratory analysis confirmed that Umary contains diclofenac and omeprazole, which are not listed on the product label. Diclofenac is a non-steroidal anti-inflammatory…
La Paix contains hidden drug ingredient
[6-14-2024] The Food and Drug Administration is advising consumers not to purchase or use La Paix, a product promoted and sold for sexual enhancement on various websites, and possibly in some retail stores. This product was discovered during an examination of imported goods. FDA laboratory analysis confirmed that La Paix contains sildenafil, the active ingredient…
Teleflex/Arrow International Recall Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits for Manufacturing Issue That May Prevent Full Balloon Inflation and Cause Patient Harm
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. Please be aware, this recall is a correction, not a product removal. Recalled Product Product Name: Arrow FiberOptix Intra-Aortic Balloon (IAB) Catheter Kit and Arrow UltraFlex Intra-Aortic Balloon Catheter…
Heinen’s Issues Allergy Alert on Undeclared Pecans in Heinen’s Tuscan Salad Bowls
Summary Company Announcement Date: May 30, 2024 FDA Publish Date: June 14, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Pecans Company Name: Heinen’s Inc. Brand Name: Brand Name(s) Heinen’s Product Description: Product Description Tuscan Salad Bowl Company Announcement May 30th, 2024. Heinen’s of Warrensville Heights, OH is voluntarily…
Electrode Pad Recall: Megadyne Removes MEGADYNE MEGA SOFT Pediatric Patient Return Electrodes for Risk of Serious Burn Injuries to Patients
This recall involves removing devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Figure 1: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode Product Name: MEGADYNE MEGA SOFT Pediatric Patient…
Villa Nueva Interservices LLC Issues Allergy Alert on Undeclared Milk in “Arepas LA Mejor” 25 oz Bags of Arepa de Choclo /Chocolo
Summary Company Announcement Date: June 11, 2024 FDA Publish Date: June 13, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Villa Nueva Interservices LLC Brand Name: Brand Name(s) Arepas La Mejor Product Description: Product Description Company Announcement Villa Nueva Interservices LLC. in Lake Worth, FL is…
Bridgewater, Vermont Man Sentenced for Conspiracy to Distribute Opioids
Department of JusticeU.S. Attorney’s OfficeDistrict of Vermont FOR IMMEDIATE RELEASETuesday, June 11, 2024 Burlington, Vermont – The United States Attorney’s Office for the District of Vermont stated that on June 10, 2024, Law Zabriskie, 66, of Bridgewater, Vermont, was sentenced by United States District Judge William K. Sessions III to a time-served sentence to be…
AAHU Barah USA Inc. Recalls Product Due to Undeclared Sulfites
Summary Company Announcement Date: May 10, 2024 FDA Publish Date: June 13, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Sulfites Company Name: AAHU BARAH USA INC. Brand Name: Brand Name(s) Aahu Barah Product Description: Product Description Apricot roll Company Announcement AAHU BARAH USA INC. of Hicksville, NY is…
Suntegrity Skincare Issues Voluntary Recall of Suntegrity Impeccable Skin Sunscreen Foundation (Multiple Shades) Due to Microbial Contamination
Summary Company Announcement Date: June 11, 2024 FDA Publish Date: June 12, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Higher than acceptable microbiological mold count Company Name: Suntegrity Skincare Brand Name: Brand Name(s) Suntegrity Product Description: Product Description Sunscreen foundation Company Announcement FOR IMMEDIATE RELEASE – Jun 11, 2024 – Las Vegas,…
Male Enhancement Supplements Recalled
Summary Company Announcement Date: February 01, 2024 FDA Publish Date: June 11, 2024 Product Type: Dietary SupplementsDrugs Reason for Announcement: Recall Reason Description Product is tainted with sildenafil and tadalafil Company Name: Integrity Products Brand Name: Brand Name(s) Ram It, To The Moon Product Description: Product Description Dietary Supplements for Male Sexual Enhancement Company Announcement…