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…
Ten Pharmaceutical Distributor Executives, Sales Representatives, and Brokers Charged in Connection with Unlawful Sales of Nearly 70M Opioid Pills
Department of JusticeOffice of Public Affairs FOR IMMEDIATE RELEASEThursday, October 3, 2024 Largest Ever Criminal Enforcement Action Targeting Distributors of Pharmaceutical Opioids and Commonly Abused Prescription Drugs with Estimated Street Value of $1.3B Charges against five pharmaceutical distributor executives and five pharmaceutical sales representatives and brokers have been unsealed in the Southern District of Texas,…
Related Recalls – Plastic Syringes Made in China for Potential Device Failures
Cypress Medical Products General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson… Sol-Millennium Medical Inc. Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M 1ml TB Syringe w/Fixed Needle 25G*5/… Sol-Millennium Medical Inc. Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml Luer Lock Syringe w… Sol-Millennium…
Infusion Pump Software Correction: Fresenius Kabi USA, LLC, Issues Correction for Ivenix Infusion System Large Volume Pump (LVP) Software due to Multiple Anomalies that May Cause Delay or Underdosage of Therapy
This recall involves correcting 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: Ivenix Infusion System (IIS) LVP Software…