Department of JusticeU.S. Attorney’s OfficeDistrict of New Hampshire FOR IMMEDIATE RELEASEMonday, October 7, 2024 CONCORD – A Northfield woman pleaded guilty today in federal court for diverting fentanyl from an ICU patient at Concord Hospital, U.S. Attorney Jane E. Young announces. Lisa Richardson, 48, pleaded guilty to one count of Tampering with Consumer Products. U.S. District…
Philips Respironics Issues Additional Usage Instructions for Trilogy Evo Ventilators Related to Use of In-Line Nebulizers
Summary Company Announcement Date: October 07, 2024 FDA Publish Date: October 07, 2024 Product Type: Medical Devices Reason for Announcement: Recall Reason Description The use of in-line nebulizers placed in certain locations may lead to aerosol deposits forming over time on the ventilator flow sensor. Should this occur, there is a possibility of inaccurate flow…
Florida Company Charged with Conspiring to Sell Misbranded N95 Masks to Hospital in Early Months of COVID-19 Pandemic
Department of JusticeU.S. Attorney’s OfficeDistrict of Massachusetts FOR IMMEDIATE RELEASEWednesday, October 2, 2024 Two individuals also charged with misbranding N95 masks and conspiracy to commit price gouging BOSTON – A Florida company, and two individuals associated with the company, have been charged and agreed to plead guilty to charges associated with shipping facemasks that were…
Resuscitator Recall: Mercury Medical Removes Neo-Tee T-Piece Resuscitators due to Risk of Inline Controller Detachment that May Impact Ventilation
This recall involves removing certain 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 Product Name: Neo-Tee T-Piece Resuscitator with manometer and controller with pressure relief valve Part Number…
Youngstown Grape Distributors Inc. Recalls Happy Moose Juice Tropical Roots and Happy Moose Strawberry Fields Because of Possible Health Risk
Summary Company Announcement Date: October 04, 2024 FDA Publish Date: October 07, 2024 Product Type: Food & Beverages Juice Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness Company Name: Youngtown Grape Distributors Inc Brand Name: Brand Name(s) Happy Moose Product Description: Product Description Tropical Roots and Strawberry Fields, 12 oz bottles Company…
Infusion Pump Correction: B. Braun Medical Inc. Issues Correction for lnfusomat Space Infusion System/Large Volume Pump, in addition to Infusomat Space Large Volume Pump Wireless, and lnfusomat Space Large Volume Pump Non-Wireless BATTERY PACK, Due to Faulty Occlusion Alarm
This recall involves correcting certain devices, and does not involve removing them 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 without correction. Affected Product Product Names: lnfusomat Space Infusion System/Large Volume…
Tracheostomy Tube Recall: Smiths Medical Removes Certain Bivona Neonatal/Pediatric and Adult Tracheostomy Tubes due to Manufacturing Defect that May Cause Tracheostomy Displacement or Decannulation
This recall involves removing certain 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 Image of torn flange due to manufacturing defect. Product Names: Bivona Aire-Cuf, TTS, Uncuffed, Mid-Range…
Bionpharma Inc. Issues Voluntary Nationwide Recall of Atovaquone Oral Suspension Due to Bacterial Contamination
Summary Company Announcement Date: September 17, 2024 FDA Publish Date: September 18, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Product found to be contaminated with Cohnella bacteria Company Name: Bionpharma Inc. Brand Name: Brand Name(s) BionPharma Product Description: Product Description Atovaquone Oral Suspension, 750 mg/mL Company Announcement FOR IMMEDIATE RELEASE – September…
Lunds & Byerlys Voluntarily Recalls L&B Lone Star Dip Due to Potential Mold
Summary Company Announcement Date: October 04, 2024 FDA Publish Date: October 04, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential mold contamination Company Name: Lunds & Byerlys Brand Name: Brand Name(s) Product Description: Product Description Lone Star Dip Company Announcement Edina, Minn. (October 4, 2024) – Lunds &…
Jacks and the Green Sprouts Recalls Alfalfa and Alfalfa Onion Sprouts Because of Possible Health Risk
Summary Company Announcement Date: October 04, 2024 FDA Publish Date: October 04, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Listeria monocytogenes Company Name: Jack and the Green Sprouts, Inc. Brand Name: Brand Name(s) Jack & the Green Sprouts Product Description: Product Description Alfalfa and Alfalfa & Onion Sprouts…