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Terminated

Digital Fluorographic System model DFP-2000A.

FDA Recall Z-0100-04 · Posted 2003-11-06

Recalling FirmToshiba American Med Sys Inc
Recall StatusTerminated
Product CodeJAA
Date Initiated2003-05-27
Date Terminated2005-03-15
Product Quantity471

Reason for Recall

Images display with wrong patient demographics.

Firm Action

Firm has issued to it''s service persons orders to install a software fix on 27 May 2003.

Root Cause

Other

Distribution Pattern

Naitonwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K941611TDA-4000/A4Toshiba America Medical Systems, In.C · 1994-05-13

Official Source

View FDA Recall →

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

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