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Terminated

Philips Brilliance CT Scanner System, 6, 10 & 16 slice images.

FDA Recall Z-0787-04 · Posted 2004-07-20

Recalling FirmPhilips Medical Systems (Cleveland) Inc
Recall StatusTerminated
Product CodeJAK
Date Initiated2004-03-08
Date Terminated2008-10-29
Product Quantity97 units

Reason for Recall

The CT couch may move downward to its lower limit without command.

Firm Action

The firm contacted their Field Service Personnel by letter on 3/8/2004. The letter instructs the field personnel to immediately install the corrective firmware kits (from Siemens) on all affected units in the field.

Root Cause

Other

Distribution Pattern

The systems were installed at medical facilities located nationwide and worldwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K012009MX8000 IDT CT SYSTEMMarconi Medical Systems, Inc. · 2001-09-13

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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