Philips Medical Systems North America Co. Phillips Practix 300 Mobile X-ray systems. The systems are used in general purpose diagnostic imaging, and are specifically used as mobile X-ray systems for bedside radiological examinations. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Practix 300 Mobile X-ray systems. The systems are used in general purpose diagnostic imaging, and are specifically used as mobile X-ray systems for bedside radiological examinations.
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
Serial numbers 4561206, 6561652, 6561768, 6561732, 6561728, 6561730, 6561767, 355142, and 06561731
Products Sold
Serial numbers 4561206, 6561652, 6561768, 6561732, 6561728, 6561730, 6561767, 355142, and 06561731
Philips Medical Systems North America Co. Phillips is recalling Practix 300 Mobile X-ray systems. The systems are used in general purpose diagnostic imaging, and a due to X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.
Recommended Action
Per FDA guidance
The firm sent letters out via certified mail from 04/03/2007 through 04/09/2007 to consignees informing them of the issue. The letter indicates that the firm plans to replace consignee's systems with the Practix Convenio Mobile X-ray System at no charge by the end of May 2007.
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