Drugs & medicalClass II

Baxter Healthcare Corporation recalls Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version:…

Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.

Read the official notice →
Date
2026-03-25
Country
United States
Brand
Baxter Healthcare
Product
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software…
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AZ, CO, IL, IN, KS,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2026-07-08
  2. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung Expansion…

    There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization,…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  3. 2026-06-10
  4. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with…

    Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower transfers of ingredients, or system…

    FDA · DeviceBaxter Healthcare CorporationWorldwide - US Nationwide distribution including in the states of Alabama,…Official notice →
  5. 2026-04-08
  6. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy…

    Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or…

    FDA · DeviceBaxter Healthcare CorporationFloridaOfficial notice →
  7. 2026-02-25
  8. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description:…

    Pumps were released without full testing being performed, including occlusion alarm testing.

    FDA · DeviceBaxter Healthcare CorporationStates: Ohio Countries: United StatesOfficial notice →
  9. 2026-02-04
  10. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Sterile Water for Irrigation, 250 mL, Single-Dose Plastic Bottle, Rx Only, Baxter Healthcare Corporation Deerfield, IL 60015 NDC:…

    Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution

    FDA · DrugBaxter Healthcare CorporationNationwideOfficial notice →
  11. 2026-01-28
  12. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls SIGMA Spectrum Infusion Pump, Model/Catalog Number: 35700BAX2

    Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective grease may lead to the device having insufficient lubrication…

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

Other drugs & medical recalls in the United States

  1. 2026-03-25
  2. US
    Drugs & medicalClass II

    Elekta, Inc. recalls Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta…

    Due to adapter not being properly aligned or locked in place.

    FDA · DeviceElekta, Inc.Worldwide - U.S. Nationwide distribution including in the states of AK, AZ,…Official notice →
  3. US
    Drugs & medicalClass II

    Stryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib, Model FL19H

    Cribs sold in the USA are missing two access door warning labels.

    FDA · DeviceStryker Medical Division of Stryker CorporationUS Nationwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft; REF#: AG740;

    Labeling mix-up resulting in the incorrect lot outer packaging of product.

    FDA · DeviceLeMaitre Vascular, Inc.US Nationwide distribution in the state of IL.Official notice →
  5. US
    Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

    A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and…

    FDA · DeviceHowmedica Osteonics Corp.Domestic: Nationwide Distribution; International: Australia, Germany, Belgium,…Official notice →
  6. US
    Drugs & medicalClass II

    GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and…

    There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized…

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

    Abbott Diagnostics Scarborough, Inc. recalls Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description:…

    It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.

    FDA · DeviceAbbott Diagnostics Scarborough, Inc.US Nationwide distribution.Official notice →
See all drugs & medical recalls →