Philips Medical Systems Nederlands: Medical Device Recall in 2019 - (Recall #: Z-1240-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are indicated for use as a diagnostic device. The purpose of the MED is to supply power to charge the magnet. MED is abbreviation for Magnet Energize Device

Product Classification:

Class II

Date Initiated: March 25, 2019

Date Posted: May 8, 2019

Recall Number: Z-1240-2019

Event ID: 82610

Reason for Recall:

Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or connected cabling.

Status: Terminated

Product Quantity: 4 units

Code Information:

US Serial Number: 47004 OUS Serial Numbers: 47001, 47002, 48000

Distribution Pattern:

US Distribution to state of: FL and Internationally to: Switzerland and Germany.

Voluntary or Mandated:

Voluntary: Firm initiated