⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Philips North America Llc: Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333

Medical DevicesSource: FDA (device) · Date: 2026-10-07

Read the official notice at FDA (device) →

Share on XFacebookRedditEmail

Get alerts for Philips North America

Guides: Which agency handles which recall (FDA vs USDA vs CPSC vs NHTSA)

The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Philips North America Llc
Product
Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
Reason / hazard
The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.
Classification
Class II
Status
Ongoing
Distribution / sold at
U.S. and U.S. Territories.
Recall initiated
2026-08-18
Code info
UDI: (01)00884838101111
Product quantity
62
Voluntary mandated
FDA Mandated
City
Cambridge
State
MA
Country
United States
Event id
99865
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.