Philips Medical Systems North America Co. Phillips View Forum 2003 software, SW 3.4L1 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
View Forum 2003 software, SW 3.4L1
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
The firm utilizes site numbers: 534544, 520177, 520633, 532261, 504927, 532134, 534573, 531862, 521928, 522027, 521424, 533804, 532053
Products Sold
The firm utilizes site numbers: 534544, 520177, 520633, 532261, 504927, 532134, 534573, 531862, 521928, 522027, 521424, 533804, 532053
Philips Medical Systems North America Co. Phillips is recalling View Forum 2003 software, SW 3.4L1 due to Automated analysis of vascular obstruction tool in software gives unreliable calibration and analysis results when using unprocessed images acquired o. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Automated analysis of vascular obstruction tool in software gives unreliable calibration and analysis results when using unprocessed images acquired on the Philips Allura FD10.
Recommended Action
Per FDA guidance
On 4/29/05 the firm mailed a letter, via certified return receipt. to their customers. The letter notified users of the problem and offered a work around. Consignees were advised they would be contacted by a representative to upgrade the unit with new software.
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