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Terminated

Diagnost 96

FDA Recall Z-1212-03 · Posted 2003-09-11

Recalling FirmPhilips Medical Systems Sales & Service Region No. America
Recall StatusTerminated
Product CodeIZZ
Date Initiated2003-08-10
Date Terminated2005-01-13
Product Quantity54

Reason for Recall

Potential for table to move by itself

Firm Action

The firm issued a letter dated 8/10/03 informing the consignees of the error and advising that a service employee will be visiting each site for software upgrade.

Root Cause

Other

Distribution Pattern

The firm distributed devices to hospitals and medical centers located throughout the U.S.

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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