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Terminated

MultiDiagnost 4 - x-ray system, multi functional/universal system for general use.

FDA Recall Z-0586-03 · Posted 2003-02-27

Recalling FirmPhilips Medical Systems
Recall StatusTerminated
Product CodeJAA
Date Initiated2003-01-10
Date Terminated2005-04-11
Product Quantity22 units

Reason for Recall

INTERNAL SHORT CIRCUIT - MAY ALLOW FOR STAND AND TABLE TO MOVE SPONTANEOUSLY IN UPWARD OR DOWNWARD MOVEMENT

Firm Action

The firm issued a letter dated January 10, 2003 to their customers advising of the problem and that a respresentative would be contacting customers to arrange a time to visit to install new interface board. This is being conducted under FCO 70800007

Root Cause

Other

Distribution Pattern

The firm distributed to 22 hospitals/medical centers located in CA, FL, IA, IL, IN, KY, MN, MO, NC, ND, NY, OH, SC, TN, TX, VA, and WV.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K961374PHILIPS MULTIDIAGNOST 4Philips Medical Systems, Inc. · 1996-08-19

Official Source

View FDA Recall →

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

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