Ventec Life Systems, Inc. recalls VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000,…
Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could result in inaccurate tidal volume monitor, not triggering on…
Read the official notice →- Date
- 2025-03-05
- Country
- United States
- Brand
- Ventec Life Systems
- Product
- VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000,…
- Classification
- Class I
- Units
- US distribution in CA, NY, and MO.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ventec Life Systems recalls
- 2026-09-30
USVentec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Labeling; Oxygen Cylinders do not contain required medical gas labeling
FDA · DeviceVentec Life Systems, Inc.US Nationwide distribution in the states of FL, IA, OH, NE, TN.Official notice →- 2026-07-01
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Ventec Life Systems, Inc. recalls VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of…
FDA · DeviceVentec Life Systems, Inc.US Nationwide distribution in the state of UT.Official notice → - 2026-05-13
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Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could…
- 2024-03-06
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Ventec Life Systems, Inc. recalls VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) REF PRT-01013-000 with pouch REF PRT-00802-001). Used with the VOCSN…
The bonded spiral wrap may detach before or during ventilation due to a manufacturing issue. Detachment of the spiral wrap can compromise structural integrity, functionality and/ or performance resulting in occlusions…
FDA · DeviceVentec Life Systems, Inc.U.S.: CA, CO, FL, HI, IN, MO, NC, and WA O.U.S.: JapanOfficial notice →
Other drugs & medical recalls in the United States
- 2025-03-05
- US
INTELERAD MEDICAL SYSTEMS INCORPORATED recalls IntelePACS (Image Fusion Module) - InteleViewer
A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on…
FDA · DeviceINTELERAD MEDICAL SYSTEMS INCORPORATEDWorldwide - US Nationwide distribution in the states of AZ, NC, MI, FL, NH,…Official notice → - US
CareFusion 303, Inc. recalls BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended…
Due to fingerprint scanner failing resulting in the scanner heating up.
FDA · DeviceCareFusion 303, Inc.Worldwide - U.S. Nationwide distribution including in the states of AL, AZ,…Official notice → - US
CareFusion 303, Inc. recalls BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis user/software/safety…
Automated dispensing device labeling is being updated to strengthen labeling around manual access to medications to address the risk of potential delays in retrieving contents/ accessing medications that may result…
FDA · DeviceCareFusion 303, Inc.US Nationwide distribution including in the states of AZ, FL, NJ, KY, GA, CA,…Official notice → - US
Turbare Manufacturing recalls Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug…
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Wuxi Medical lnstrument Factory Co., Ltd. recalls ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per…
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
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Padagis US LLC recalls Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only, For Topical Use Only, Manufactured by Padagis, Yeruham, Israel, NDC:…
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