Becton Dickinson & Company: Medical Device Recalls in 2022

According to to data from the FDA, there were 14 medical device recalls made by Becton Dickinson & Company in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system. Catalog Number: 515304
• BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog Number: 364902, 36490200
• BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
• BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
• Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.383682 (OUS)
• BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)
• BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
• BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)
• BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)
• BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
• Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
• BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
• BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
• BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)