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Terminated

Multidiagnost 96

FDA Recall Z-1204-03 · Posted 2003-09-12

Recalling FirmPhilips Medical Systems
Recall StatusTerminated
Product CodeIZZ
Date Initiated2002-02-20
Date Terminated2005-04-11
Product Quantity48 units

Reason for Recall

Spontaneous movement of table without input from an operator

Firm Action

On 2/20/02 the firm issued Field Change Order to their field personnel, instructing them to visit each site and upgrade each unit.

Root Cause

Other

Distribution Pattern

The firm distributed units to hospitals and medical centers located throughout the US.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K912470PHILIPS DIAGNOST 96Philips Medical Systems, Inc. · 1991-08-07

Official Source

View FDA Recall →

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

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