Becton Dickinson Infusion Therapy Systems, Inc. recalls BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV…
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 -…
Read the official notice →- Date
- 2025-05-28
- Country
- United States
- Brand
- Becton Dickinson Infusion Therapy Systems
- Product
- BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter 20GX1.00IN STRAIGHT BC,…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of IN, AL, CA, FL, TX,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Becton Dickinson Infusion Therapy Systems recalls
- 2025-07-02
USBecton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
FDA · DeviceBecton Dickinson Infusion Therapy Systems, Inc.Worldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →- 2024-08-07
- US
Becton Dickinson Infusion Therapy Systems, Inc. recalls BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25…
Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.
- 2023-12-06
- US
Becton Dickinson Infusion Therapy Systems Inc. recalls BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533
Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and…
FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.US Nationwide distribution in the states of CA, NC, MI, WA, CO, FL, NJ, NM,…Official notice → - 2023-10-11
- US
Becton Dickinson Infusion Therapy Systems Inc. recalls REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min ,…
There is the potential that the safety shield may not properly engage on IV catheters. The needle can pull through the safety shield and disconnect from the needle safety shield leaving the contaminated needle point…
FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.US Nationwide distribution in the states of CA, FL, GA, MA, MN, MO, MS, NJ,…Official notice → - 2022-11-09
- US
Becton Dickinson Infusion Therapy Systems Inc. recalls BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)
During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).
FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.U.S.: New York, Florida, Maryland, North Carolina, Virginia, Georgia, Rhode…Official notice → - 2021-12-01
- US
Becton Dickinson Infusion Therapy Systems Inc. recalls BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min…
There is a breach in the product packaging that renders the product non-sterile.
FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.U.S. Nationwide Distribution: AR, AZ, MA, GA, NC, OH, WA, NY, NJ, HI, CA, MD,…Official notice →
Other drugs & medical recalls in the United States
- 2025-06-04
- US
Alembic Pharmaceuticals Limited recalls Bromfenac Ophthalmic Solution 0.09%, 1.7 mL bottle, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc.,…
Failed Impurities/Degradation Specifications
- 2025-05-28
- US
Advanced Bionics, LLC recalls HiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607
Due to incorrect the battery charger being packaged and distributed. Product labeling does not match the intended product as specified.
- US
Copan WASP recalls PhenoMATRIX
AI-powered bacterial culture plate interpretation and workup software does not have Premarket Approval or pre-market notification (510(k)/de novo), so there is potential risk that the colony count and/or morphology…
FDA · DeviceCopan WASPUS: Nationwide distribution in the states of UT, AR, CA, PA, MD, NC, IL, MA,…Official notice → - US
Echopixel, Inc. recalls TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0, 1.25, and 1.35 The t3D-Viewer is designed for use by health care…
Imaging system data may be displayed with an incorrect orientation (sidedness) where the patient side is not correct (left, right, superior, inferior, anterior or posterior). This may lead to an inaccurate measurements.
FDA · DeviceEchopixel, Inc.Worldwide - U.S. Nationwide distribution in the states of CA, OH, NJ, PA, MA,…Official notice → - US
Smith & Nephew, Inc. recalls META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw,…
FDA · DeviceSmith & Nephew, Inc.Worldwide - US Nationwide distribution in the states of FL, NH, TX, CA, OH,…Official notice → - US
Philips North America Llc recalls Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Andorra,…Official notice →