FDA evaluating plastic syringes made in China – Full Alert
“The FDA received information about quality issues associated with several Chinese manufacturers of syringes. We are concerned that certain syringes manufactured in China may not provide consistent and adequate quality or performance” FDA (2023).
FDA announce Alaris infusion pump recall – Full Alert
“Becton Dickinson (BD)/Carefusion 303 is recalling their Alaris Infusion Pumps due to compatibility issues with Cardinal Health Monoject syringes” FDA (2023).
FDA announce Sapphire IV pump recall – Full Alert
“Eitan Medical Ltd is recalling the Sapphire MT Infusion Pump, Sapphire Epidural Infusion Pump, and Sapphire Plus Infusion Pump due to software issues in software version Rev 16.10” FDA (2023).
Outpatient infusion clinic patient satisfaction survey – Full Text
“The pilot survey (N = 43) revealed that patients were relatively dissatisfied with walking to clinics, lack of access to public transit, lack of parking and/or free parking, lack of privacy, and flexible scheduling and/or cancellation policies” Hu et al (2022).
UEDVT in pediatric critical care settings – Full Text
“The fusion model, which achieves better performance in CRT prediction, can better understand the risk factors for CRT and provide potential biomarkers and measures for thromboprophylaxis in pediatric intensive care settings” Li et al (2022).
Local anesthetics for IV catheter insertion
“This study aimed to investigate feasibility and potential efficacy of local anesthetics on pain intensity during PIVC insertion in an unblinded, single-center, randomized clinical pilot trial” Lozano et al (2021).
FDA recall ultrasound gel manufactured by Eco-Med – Full Alert
“As of Aug. 31, 2021, there have been at least 66 infections, including 60 bloodstream infections associated with these affected products, per the Centers for Disease Control and Prevention (CDC)” FDA (2021).
Medical devices sterilised by Steril Milano – UK Alert
“Fraudulent activity by this third-party sterilisation provider has been identified. Multiple medical device manufacturers are affected. Manufacturers are advising customers of actions required to mitigate risks” MHRA (2021).
Smiths Medical and Ivenix partner to revolutionize infusion management
“Smiths Medical, a global medical device leader, today announced it has formed an exclusive partnership with Ivenix, Inc. that positions the companies as the first in the U.S. to offer a comprehensive suite of infusion management solutions to meet healthcare needs across the continuum of care” Ivenix and Smiths Medical (2021).
Sagent Pharmaceuticals issues recall of phenylephrine hydrochloride injection – Full Alert
“Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of three lots of Phenylephrine Hydrochloride Injection, USP (10 mg/mL)” FDA (2021).
Combat Medical Systems recalls transfusion set due to possible broken needles – Full Alert
“Combat Medical is recalling the convenience kits because the needle in the blood pack may bend or disconnect from the blood bag” FDA (2021).
Field Safety Notice for BD Venflon Pro Safety needle protected IV cannula – UK Alert
“BD has confirmed an increase in reports for leakage from the injection port of the BD VenflonTM Pro Safety (VPS) Needle Protected I.V. Cannula” BD (2021).
Smiths Medical recalls Medfusion 3500 and 4000 syringe pumps – Full Alert
“Smiths Medical is recalling specific software versions of the Medfusion 3500 and 4000 Syringe Pumps because of a software error that may lead to over-delivery or under-delivery of fluids or medication” FDA (2021).
Misconnection events leading to wrong-route medication errors – Full Text
“These case reports confirm that misconnection events leading to wrong-route errors can occur and may cause serious injury” Viscusi et al (2020).
Important safety information regarding cleaning practices of Sigma Spectrum infusion pumps – Full Text
“To date, Baxter has received 16 reports of serious injuries that may have resulted from improper cleaning practice-related residue buildup and/or corrosion” FDA (2020).
The process of agreeing to CVAD placement for IV chemotherapy administration
“Overall, the results of the study showed that the DCS-ITA is a psychometrically sound instrument that easily discriminates between patients who are experiencing a decisional conflict and those who are not” Esposito et al (2020).
PICC-related bloodstream infection in patients with eating disorders
“In patients with eating disorder treated with nutritional therapy using a PICC, prolonged resistance to weight gain became a risk factor for developing CRBSI” Tamura et al (2020).
Becton Dickinson (BD) CareFusion 303 Inc. recalls Alaris™ syringe and Alaris™ PCA modules – Full Alert
“Becton Dickinson (BD) CareFusion 303 Inc. Recalls Alaris™ Syringe and Alaris™ PCA Modules Due to Potential Incorrect Display of Syringe Types and/or Sizes” FDA (2020).
Becton Dickinson (BD) CareFusion 303, Inc. Recalls Alaris™ System PC Unit – Full Alert
“Becton Dickinson (BD) CareFusion 303, Inc. Recalls Alaris™ System PC Unit and PC Unit Front Case Keypad Replacement Kits Due to Risk of Stuck or Unresponsive Keys” FDA (2020).
Becton Dickinson (BD) CareFusion 303 recalls Alaris System Infusion Pumps – Full Alert
“Becton Dickinson (BD) CareFusion 303 Recalls Alaris System Infusion Pumps Due to Damaged Inter-Unit Interface Connectors, Loose or Missing Battery Screws and A Broken Upper and Lower Hinge Posts and Membrane Frame” FDA (2020).
BD provides update on previously disclosed recall of BD Alaris system hardware
“BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today provided an update on a previously announced voluntary recall of the BD Alaris™ System” FDA (2020).
Recall of ChloraPrep 3 mL applicator in specific US territories and countries
“Voluntary recall on June 23, 2020 of the ChloraPrep™ 3 mL applicator due to possible fungal contamination” FDA (2020).
Smiths medical recalls Medfusion 3500 and 4000 syringe pumps
“Smiths Medical is recalling specific software versions of the Medfusion 3500 and 4000 Syringe Pumps because of a software error” FDA (2020).
Smiths Medical partners with U.S. government on COVID-19 vaccine efforts – Full Text
“Smiths Medical has received an order through our authorized distributor Marathon Medical’s BARDA IDIQ agreement for 78.6 million syringe and needle units’ Smiths Medical (2020).
Interview on how TournIQ is revolutionizing IV access – Full Text
“Stockholm-based Ortrud Medical has designed TournIQ, a tourniquet that helps the user apply optimal pressure on the arm to increase vein visibility, palpability, and size when gaining IV access” Medgadget (2020)
FDA approves ivWatch to monitor IV sites for leakage – Full Text
“ivWatch, a company based in Newport News, Virginia, won FDA clearance for its SmartTouch sensor that detects peripheral IV infiltration and extravasation events” Medgadget (2020).
ECRI advice on COVID-19 and the use of infusion pumps with long extension sets – Full Text
“In some cases, infusion pumps can be used with extension sets outside of the patient room to protect the clinical personnel and conserve personal protective equipment” ECRI (2020).
B. Braun receives FDA emergency use authorization for use of infusion pumps with nebulizers for COVID-19 patients
“Studies have shown that using infusion pumps with nebulizers can help provide steady, controlled delivery of nebulized medication to patients with acute respiratory distress syndrome (ARDS). Some of the most critical COVID-19 patients suffer from severe ARDS” B. Braun (2020).
Considerations on the use of vascular access devices in patients with COVID-19
“Document was released on April 5, 2020 by a group of experts from the Long Term Central Venous Access Group (GAVeCeLT) and covers important aspects of vascular access in COVID-19 patients, based on their current experience in the treatment of these patients” GAVeCeLT (2020).
BD recalls Alaris system infusion pumps due to software and system errors
“BD/CareFusion 303 is recalling the Alaris Infusion Pump System and Modules due to multiple system errors, software errors, and use-related errors” FDA (2020).