Date Issued: September 29, 2021 The U.S. Food and Drug Administration (FDA) is warning consumers about the potential risk of injury associated with the use of the Safe-T-Lite UV WAND, manufactured by Max-Lux Corporation Limited. Use of Max-Lux Safe-T-Lite UV WAND may expose the user or any nearby person to unsafe levels of ultraviolet-C (UV-C)…
Cuisine Innovations Unlimited, LLC Issues Allergy Alert on Undeclared Egg Yolks in “Vemondo Vegan Crabless Mini Crabcakes” by Lidl
Summary Company Announcement Date: September 28, 2021 FDA Publish Date: September 28, 2021 Product Type: Food & Beverages Seafood/Seafood Product Allergens Reason for Announcement: Recall Reason Description Undeclared egg yolks Company Name: Cuisine Innovations Unlimited, LLC Brand Name: Brand Name(s) Vemondo by Lidl Product Description: Product Description Vegan Crabless Mini Crabcakes Company Announcement Cuisine Innovations…
Allergy Alert on Undeclared Wheat in Cheese Curds and Ice Cream
Summary Company Announcement Date: September 27, 2021 FDA Publish Date: September 27, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared wheat Company Name: Picket Fence Creamery, LLC Brand Name: Brand Name(s) Picket Fence Creamery, LLC Product Description: Product Description taco white cheddar cheese curds and key lime pie ice cream…
Left Atrial Appendage Occlusion (LAAO) Devices Potentially Associated with Procedural Outcome Differences Between Women and Men – Letter to Health Care Providers
September 27, 2021 The U.S. Food and Drug Administration (FDA) is informing health care providers of recent information about the potential for differences in procedural outcomes between women and men undergoing implant of a left atrial appendage occlusion (LAAO) device. The FDA is evaluating a study published in the Journal of the American Medical Association…
Eli Lilly and Company Issues Voluntary Nationwide Recall of One Lot of GLUCAGON® Emergency Kit Due to Loss of Potency
Summary Company Announcement Date: September 25, 2021 FDA Publish Date: September 26, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Loss of potency Company Name: Eli Lilly and Company Brand Name: Brand Name(s) Product Description: Product Description Glucagon Emergency Kit Company Announcement Eli Lilly and Company (NYSE: LLY) is voluntarily recalling lot D239382D,…
Suntree Snack Foods, LLC. Issues Voluntary Recall of Roasted Salted Cashew Halves & Pieces and Trail Mix Containing Roasted Salted Cashews Due to Potential Presence of Glass Pieces
Summary Company Announcement Date: September 24, 2021 FDA Publish Date: September 24, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential presence of glass pieces. Company Name: SunTree Snack Foods, LLC Brand Name: Brand Name(s) Multiple brand names Product Description: Product Description Roasted salted cashew halves & pieces and trail mix…
Allergy Alert Issued for Undeclared Milk and Egg in Apple and Cherry Pies Sold at Five Whole Foods Market Stores in Mid-Atlantic Region
Summary Company Announcement Date: September 24, 2021 FDA Publish Date: September 24, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk and eggs Company Name: Whole Foods Market Brand Name: Brand Name(s) Whole Foods Market Product Description: Product Description Apple Pie and Cherry Pie Company Announcement Whole Foods Market is…
Armstrong Medical Limited Recalls AMSORB PLUS PREFILLED G-CAN 1.0L Due to Reduced Gas Flow to Patients During Anesthesia
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 AMSORB PLUS PREFILLED G-CAN 1.0L Product Codes and Lot Numbers: See Recall Database Entry Devices Recalled in the United States: 214,032 Distribution Date: October 22, 2020 to…
Cordis Recalls SUPER TORQUE MB Angiographic Catheter with Radiopaque Marker Bands Due to Potential for Marker Bands to Move or Dislodge
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 Cordis SUPER TORQUE MB Angiographic Catheter with Radiopaque Marker Bands Lot Numbers: See Database Entry Distribution Dates: January 1, 2019 to July 20, 2021 Devices Recalled in the…
IntegraDose Compounding Services, LLC Issues Voluntary Nationwide Recall of Cefazolin Injection Products Due to a Lack of Sterility Assurance
Summary Company Announcement Date: September 20, 2021 FDA Publish Date: September 21, 2021 Product Type: Drugs Pharmaceutical Quality Reason for Announcement: Recall Reason Description Lack of sterility assurance. Company Name: IntegraDose Compounding Services, LLC Brand Name: Brand Name(s) IntegraDose Compounding Services, LLC Product Description: Product Description Company Announcement Minneapolis, Minnesota, IntegraDose Compounding Services is voluntarily…