Philips Medical Systems Easy Access Software releases 1.1, 5.2, 6.2 & 7.2 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Easy Access Software releases 1.1, 5.2, 6.2 & 7.2
Brand
Philips Medical Systems
Lot Codes / Batch Numbers
The firm utilizes a site # to identify the devices: 83966, 82846, 82847, 82843, 82845, 82850, 82849, 82844, 102836, 76904, 103125, 103124, 102835, 100640, 101185, 76938, 85078, 76937, 85083, 85077, 76904, 86255, 87121, 87120, 87119, 84399, 10276, 85052, 86190, 86050, X1758, X1676, 84031, 83966, 86002, 86001, X1776, 84476, 84088, 83676, 85451, 84361, 76945, 87130, 86198, 10379
Products Sold
The firm utilizes a site # to identify the devices: 83966, 82846, 82847,82843, 82845, 82850, 82849, 82844, 102836, 76904, 103125, 103124, 102835, 100640, 101185, 76938, 85078, 76937, 85083, 85077, 76904, 86255, 87121, 87120, 87119, 84399, 10276, 85052, 86190, 86050, X1758, X1676, 84031, 83966, 86002, 86001, X1776, 84476, 84088, 83676, 85451, 84361, 76945, 87130, 86198, 10379
Philips Medical Systems is recalling Easy Access Software releases 1.1, 5.2, 6.2 & 7.2 due to If DICOM fields for body part, description or accession number are changed, change won't update on the EasyWeb client or hospital systems.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If DICOM fields for body part, description or accession number are changed, change won't update on the EasyWeb client or hospital systems.
Recommended Action
Per FDA guidance
On 6/25/03 the firm issued a letter dated 6/15/03 to the affected customers. The letter advises of the problem and advises the customer that the firm will install corrected software in affected units.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026