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…
Read the official notice →- Date
- 2023-12-06
- Country
- United States
- Brand
- Becton Dickinson Infusion Therapy Systems
- Product
- BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533
- Classification
- Class II
- Units
- US Nationwide distribution in the states of CA, NC, MI, WA, CO, FL, NJ, NM,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 →- 2025-05-28
- US
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 -…
FDA · DeviceBecton Dickinson Infusion Therapy Systems, Inc.Worldwide - US Nationwide distribution in the states of IN, AL, CA, FL, TX,…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.
- 2023-10-11
- 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
- 2023-12-06
- US
Intuitive Surgical, Inc. recalls Da Vinci Single-Site Wristed Needle Driver, REF: 478115, 5 mm
There is the potential for the needle drive to become dislodged and/or broken which could result in uncontrollable movement.
FDA · DeviceIntuitive Surgical, Inc.US: IL, FL, ID, SC, MI, TX, TN, NY, OR, CO, CA, MS, NJ, Puerto Rico OUS: South…Official notice → - US
Breas Medical, Inc. recalls with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits: 006093, 006653, an accessory to ventilator device, Vivo 45LS.…
Produced with unintended open slits on the side of the mouthpiece body, may result in insufficient ventilation in spontaneous breathing patients using MPV-VCV and MPV-PCV modes of ventilation
- US
PATH recalls SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S
Affected lots of product may experience technical distortions to a greater extent than expected.
- US
Botanical Be recalls Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol…
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
- US
Bayer Healthcare Pharmaceuticals Inc. recalls VITRAKVI (larotractenib) oral solution, 20mg/mL, 100 mL bottle, Rx only, Manufactured for Bayer HealthCare Pharmaceuticals…
Microbial Contamination of Non-Sterile Products: microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing
FDA · DrugBayer Healthcare Pharmaceuticals Inc.Product was distributed to specialty pharmacies and distributors nationwide…Official notice → - US
Golden State Medical Supply Inc. recalls PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bottle NDC 60429-734-90;…
Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine