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Philips Medical Systems Nederlands recalls Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems a
Recalled May 8, 2019 · FDA recall Z-1240-2019 · Philips Medical Systems Nederlands
Hazard
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. · FDA Class II
Units
4 units
Sold at
US Distribution to state of: FL and Internationally to: Switzerland and Germany.
Description
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.
Product
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
Manufacturer(s)
Philips Medical Systems Nederlands
Made in
Netherlands
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →