medical MODERATE Updated 2026-10-07

Volcano Corp recalls Philips IntraSight Plus REF: 797423 and 797417 100-120v-22

See all recalls from Volcano Corp →

Recalled Product

Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: REF: 797423:(01)00845225012946/REF:797417: (01)00845225012939 all Philips IntraSight Plus Systems with Software Version 6.0.4

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Philips IntraSight Plus →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Philips North America recalls SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T

2026-10-07 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.

Karl Storz Endoscopy recalls HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 0404855

2026-10-07 · Due to incorrect inside packaging label for eyepiece.

ASP Global, LLC. recalls Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET C

2026-10-07 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

ASP Global, LLC. recalls Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15"

2026-10-07 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.