Philips Medical Systems North America Co. Phillips AD5 table, modified, used with the XPER x-ray systems. The modification on the table is the cables used for connecting to the XPER systems. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AD5 table, modified, used with the XPER x-ray systems. The modification on the table is the cables used for connecting to the XPER systems.
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
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Products Sold
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Philips Medical Systems North America Co. Phillips is recalling AD5 table, modified, used with the XPER x-ray systems. The modification on the table is the cables due to Potential for high voltage exposure involving the injector interface connector of patient support tables.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for high voltage exposure involving the injector interface connector of patient support tables.
Recommended Action
Per FDA guidance
On 10/10/05 the firm issued a letter to customers alerting customers to the problem and advising that the firm will perform an upgrade to the devices at customer sites. In March 2006 the firm issued a second notification letter involving more 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