Class IIOngoingZ-2002-2025
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381433
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson Infus…UTJul 2, 2025
Recalls in Utah
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 49–60 of 62 recalls
Class IIOngoingZ-2001-2025
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381533
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson Infus…UTJul 2, 2025
Class IIOngoingZ-2000-2025
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 382633
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson Infus…UTJul 2, 2025
Class IIOngoingZ-1999-2025
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381423
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson Infus…UTJul 2, 2025
Class IIOngoingZ-1877-2025
BioFire Diagnostics, LLC recalls BioFire Respiratory Panel 2.1 plus Kit
Due to manufacturing error, respiratory panel may result in elevated control failures and/or false negative results.
BioFire Diagnostics, L…UTJun 4, 2025
Class IIOngoingZ-1808-2025
Becton Dickinson Infusion Therapy Systems, Inc. recalls BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN
Due to a manufacturing defect IV catheter may have a hole in the septum, which may result in blood leakage from the septum during insertion, which may cause blood exposure or the need for a second IV to be placed - which…
Becton Dickinson Infus…UTMay 28, 2025
Class IIOngoingZ-1641-2025
Merit Medical Systems, Inc. recalls Merit Medical
Update to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.
- Gastroesophageal Reflux Disease (Gerd) Endoscopic Suture/Plication System
- Under Investigation by firm
Merit Medical Systems,…UTApr 30, 2025
Class IIOngoingZ-1640-2025
Merit Medical Systems, Inc. recalls Merit Medical
Update to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.
- Gastroesophageal Reflux Disease (Gerd) Endoscopic Suture/Plication System
- Under Investigation by firm
Merit Medical Systems,…UTApr 30, 2025
Class IOngoingZ-1507-2025
Bard Access Systems, Inc. recalls BD 4 Fr Single-Lumen PowerPICC Catheters
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to i…
Bard Access Systems, I…UTApr 23, 2025
Class IIOngoingZ-1518-2025
BioFire Diagnostics, LLC recalls FilmArra Pneumonia Panel plus (Pneumoplus)
Increased risk of control failures and false negative test results with multiplexed nucleic acid test.
- Mers-Cov And Common Respiratory Pathogens Semi-Quantitative And Quantitative Multiplex Nucleic Acid Detection System
- Nonconforming Material/Component
BioFire Diagnostics, L…UTApr 16, 2025
Class IIOngoingZ-1434-2025
Merit Medical Systems, Inc. recalls Prelude IDEAL 4 F Hydrophilic Sheath Introducer
Hydrophilic Sheath Introducer labeled for 4F dilators may instead incorrectly contain 5F dilators. Incorrect dilator use may result in procedure delay.
Merit Medical Systems,…UTApr 2, 2025
Class IIOngoingZ-1235-2025
Scientia Vascular, Inc. recalls Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices…
Due to manufacturing non-conformance that resulted in channels in the seal on the packaging pouch. As a result, this could potential create a breach in the sterile barrier.
Scientia Vascular, Inc…UTMar 5, 2025