Drugs & medicalClass II

Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor (CVSM):

There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.

Read the official notice →
Date
2025-04-23
Country
United States
Brand
Baxter Healthcare
Product
Welch Allyn Connex Vital Signs Monitor (CVSM):
Classification
Class II
Units
Worldwide - US Nationwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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 Baxter Healthcare recalls

  1. 2025-05-28
  2. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

    There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.

    FDA · DeviceBaxter Healthcare CorporationUS and CanadaOfficial notice →
  3. 2025-05-21
  4. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

    A cybersecurity vulnerability was discovered through internal testing.

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
  5. 2025-04-23
  6. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A; 2) ) Product Code/Part…

    Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
  7. 2025-04-02
  8. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility,…

    The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide. Global Distribution.Official notice →
  9. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

    Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to…

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of AR, CA, FL, IA, IN, LA, MO, MT,…Official notice →
  10. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087

    There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution.Official notice →
All 123 Baxter Healthcare recalls →

Other drugs & medical recalls in the United States

  1. 2025-04-23
  2. US
    Drugs & medicalClass II

    Conformis Inc. recalls restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for Cordera Hip System

    The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.

    FDA · DeviceConformis Inc.US Nationwide distribution in the states of CA, FL, NV, TN.Official notice →
  3. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A; 2) ) Product Code/Part…

    Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Straumann USA LLC recalls TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel; REF: 037.3002;

    The devices are missing the laser marked depth markings.

    FDA · DeviceStraumann USA LLCWorldwide - US Nationwide distribution in the states of CA, IN, ME, MN and the…Official notice →
  5. US
    Drugs & medicalClass II

    Abbott Medical recalls Aveir DR Leadless Pacemaker (LP) Ventricular Device REF LSP202V UDI-DI code: 05415067040725 REF LSP112V UDI-DI code: 05415067034472 The…

    Due to a manufacturing issue, leadless pacemakers may have been exposed to higher than normal temperatures which may result in premature battery failure.

    FDA · DeviceAbbott MedicalWorldwide - U.S. Nationwide distribution in the states of FL, SC, and WV and…Official notice →
  6. US
    Drugs & medicalClass II

    GE Medical Systems, LLC recalls Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG,…

    The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

    FDA · DeviceGE Medical Systems, LLCWorldwide - US Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Philips North America Llc recalls Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.

    Potential for collimator to fall as a result of incorrect installation.

    FDA · DevicePhilips North America LlcWorldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH,…Official notice →
See all drugs & medical recalls →