Official recall record
Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the interna
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-09-03
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00884838099739
- Brand on record
- Philips North America Llc
What the authority reported
Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may include anxiety of a patient is left on the tabletop inside the bore for a longer duration than anticipated. movement.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 3 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2025-05-13 · US FDA — Medical Devices
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143; - 2024-04-22 · US FDA — Medical Devices
Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated fo - 2025-06-30 · US FDA — Medical Devices
Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;