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Terminated

GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d) 2052782-00x

FDA Recall Z-1781-2019 · Posted None

Recalling FirmGE Healthcare, LLC
Recall StatusTerminated
Product CodeLLZ
Date Initiated2019-05-22
Date Terminated2024-09-20
Product Quantity620 units

Reason for Recall

There is a potential that one or more image series (i.e., all images within an image set) may be missing from an exam without a warning displayed in the viewer.

Firm Action

The firm initiated their medical device correction by letter on 05/2/2019. The letter explained the problem and the safety issue and provided the following safety instructions: 1) Process Root Causes: Investigation determined that the original PACS-IW foundation design did not incorporate adequate risk mitigation for this part of the image ingestion process. DFMEA of the image ingestion wing to wing process was completed as part of the investigation, and no additional areas where further mitigations are required were identified. a) If a discrepancy is identified, attempt to retransmit the exam to PACS. b) If retransmission is unsuccessful, contact a GE Healthcare Service representative for assistance in resolving the impacted exam. c) Urgent cases impacted by this issue should be interpreted by the clinician at the modality. 2) Be aware that if DICOM storage commit is configured and in use, the modality will not be sent a commit notification for images impacted by this issue. 3) Attention should be given to prior cases, acquired before the application of the safety instructions given in this communication, because they may be affected by this issue. For historical data inquiries, please contact a GE Healthcare service representative for assistance in identifying any affected images. The units will be upgraded.

Root Cause

Software design

Distribution Pattern

Worldwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

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

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